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Alopecia‐mental retardation syndrome: Molecular genetics of a rare neuro‐dermal disorder

Annals of human genetics, 2021-09, Vol.85 (5), p.147-154

2021

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Optimizing Spectrum Utilization and Security in SAS-Enabled CBRS Systems for Enhanced 5G Performance

IEEE access, 2024, Vol.12, p.1-1

2024

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Secured Dynamic Request Scheduling and Optimal CSP Selection for Analyzing Cloud Service Performance Using Intelligent Approaches

IEEE access, 2023, Vol.11, p.140914-140933

2023

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Exome sequence analysis identifies a homozygous, pathogenic, frameshift variant in the MAN2B1 gene underlying clinical variant of α-mannosidosis

Frontiers in genetics, 2024-08, Vol.15, p.1421943

2024

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Analysis of a non‐lethal biallelic frameshift mutation in ZMPSTE24 reveals utilization of alternative translation initiation codons

Clinical genetics, 2023-10, Vol.104 (4), p.491-496

2023

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Machine Learning Approach to Classification of Online Users by Exploiting Information Seeking Behavior

IEEE access, 2024-01, Vol.12, p.1-1

2024

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An exceptional biallelic N-terminal frame shift mutation in ZMPSTE24 leads to non-lethal progeria due to possible utilization of a downstream alternative start codon

Gene, 2022-07, Vol.833, p.146582-146582, Article 146582

2022

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Current updates on genetic spectrum of usher syndrome

Nucleosides, nucleotides & nucleic acids, 2024-05, p.1-24

2024

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Comment on homozygosity mapping of a consanguineous Pakistani family affected with oculocutaneous albinism to Tyrosinase gene

International journal of ophthalmology, 2017-05

2017

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Autosomal recessive variants c.953A>C and c.97-1G>C in NSUN2 causing intellectual disability: a molecular dynamics simulation study of loss-of-function mechanisms

Frontiers in neurology, 2023-05, Vol.14, p.1168307-1168307

2023

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Development and Evaluation of Essential Oil-Based Nanoemulgel Formulation for the Treatment of Oral Bacterial Infections

Gels, 2023-03, Vol.9 (3), p.252

2023

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UHPLC, ATR-FTIR analysis of Nymphoides indica rhizome extract and determination of antioxidant & antibiofilm potential

Main group chemistry, 2022-01, Vol.21 (1), p.157-166

2022

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A novel homozygous TSGA10 missense variant causes acephalic spermatozoa syndrome in a Pakistani family

Basic and clinical andrology, 2024-02, Vol.34 (1), p.4-4, Article 4

2024

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Computational analyses of RPIA gene mutation causing Ribose-5-phosphate isomerase deficiency: a rarest known metabolic disorder in humans

Journal of Taibah University for Science, 2023-12, Vol.17 (1)

2023

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A clinical and molecular characterization of a Pakistani family with multicentric osteolysis, nodulosis and arthropathy (MONA) syndrome

Bone Reports, 2024-09, Vol.22, p.101789, Article 101789

2024

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Lumateperone Interact with S-Protein of Ebola Virus and TIM-1 of Human Cell Membrane: Insights from Computational Studies

Applied sciences, 2022-09, Vol.12 (17), p.8820

2022

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Mutation Analysis of a Pakistani Oculocutaneous Albinism Family Identifies a Novel Splice Site Defect in OCA2 Gene

Pakistan journal of zoology, 2022-06, Vol.54 (3), p.1215

2022

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CHONDROMATOUS MASS ON LOWER FOREARM

Gomal journal of medical sciences, 2017-12, Vol.15 (2)

2017

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Survey of Plant Parasitic Nematodes in Different Regions of Khyber- Pakhtun-Khwa

Pakistan journal of zoology, 2015-08, Vol.47 (4)

2015

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Prioritization of Disease Prone Exons in INPP5E Gene, Associated With Joubert Syndrome, by in silico Analysis of Non-Synonymous SNPs

Pakistan journal of zoology, 2015-06, Vol.47 (3)

2015

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Mutations in the Alpha 1,2-Mannosidase Gene, MAN1B1, Cause Autosomal-Recessive Intellectual Disability

American journal of human genetics, 2011-08, Vol.89 (2), p.348-348

2011

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CLINICAL PRESENTATION OF AN EXTENDED CONSANGUINEOUS FAMILY INHERITING WOOLLY HAIR HYPOTRICHOSIS

Gomal journal of medical sciences, 2018-12, Vol.16 (1), p.24

Khan, Muzammil Ahmad

2018

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The molecular genetics of human appendicular skeleton

Molecular genetics and genomics : MGG, 2022-09, Vol.297 (5), p.1195-1214

2022

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IMAGES IN CLINICAL MEDICINE

Gomal journal of medical sciences, 2018-03, Vol.16 (1), p.24

2018

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MICROPHTHALMIA: AN IMPORTANT GENETIC EYE DISORDER

Gomal journal of medical sciences, 2017-01, Vol.14 (3)

Muzammil Ahmad Khan

2017

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Alopecia‐mental retardation syndrome: Molecular genetics of a rare neuro‐dermal disorder

Optimizing Spectrum Utilization and Security in SAS-Enabled CBRS Systems for Enhanced 5G Performance

Secured Dynamic Request Scheduling and Optimal CSP Selection for Analyzing Cloud Service Performance Using Intelligent Approaches

Exome sequence analysis identifies a homozygous, pathogenic, frameshift variant in the MAN2B1 gene underlying clinical variant of α-mannosidosis

Analysis of a non‐lethal biallelic frameshift mutation in ZMPSTE24 reveals utilization of alternative translation initiation codons

Machine Learning Approach to Classification of Online Users by Exploiting Information Seeking Behavior

An exceptional biallelic N-terminal frame shift mutation in ZMPSTE24 leads to non-lethal progeria due to possible utilization of a downstream alternative start codon

Current updates on genetic spectrum of usher syndrome

Comment on homozygosity mapping of a consanguineous Pakistani family affected with oculocutaneous albinism to Tyrosinase gene

Autosomal recessive variants c.953A>C and c.97-1G>C in NSUN2 causing intellectual disability: a molecular dynamics simulation study of loss-of-function mechanisms

Development and Evaluation of Essential Oil-Based Nanoemulgel Formulation for the Treatment of Oral Bacterial Infections

UHPLC, ATR-FTIR analysis of Nymphoides indica rhizome extract and determination of antioxidant & antibiofilm potential

A novel homozygous TSGA10 missense variant causes acephalic spermatozoa syndrome in a Pakistani family

Computational analyses of RPIA gene mutation causing Ribose-5-phosphate isomerase deficiency: a rarest known metabolic disorder in humans

A clinical and molecular characterization of a Pakistani family with multicentric osteolysis, nodulosis and arthropathy (MONA) syndrome

Lumateperone Interact with S-Protein of Ebola Virus and TIM-1 of Human Cell Membrane: Insights from Computational Studies

Mutation Analysis of a Pakistani Oculocutaneous Albinism Family Identifies a Novel Splice Site Defect in OCA2 Gene

CHONDROMATOUS MASS ON LOWER FOREARM

Survey of Plant Parasitic Nematodes in Different Regions of Khyber- Pakhtun-Khwa

Prioritization of Disease Prone Exons in INPP5E Gene, Associated With Joubert Syndrome, by in silico Analysis of Non-Synonymous SNPs

Mutations in the Alpha 1,2-Mannosidase Gene, MAN1B1, Cause Autosomal-Recessive Intellectual Disability

CLINICAL PRESENTATION OF AN EXTENDED CONSANGUINEOUS FAMILY INHERITING WOOLLY HAIR HYPOTRICHOSIS

The molecular genetics of human appendicular skeleton

IMAGES IN CLINICAL MEDICINE

MICROPHTHALMIA: AN IMPORTANT GENETIC EYE DISORDER

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