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Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...Journal of inherited metabolic disease, 2020-11, Vol.43 (6), p.1333-1348
- Ng, Bobby G.
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- Chen, Jian
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- Hicks, M John
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Proceedings of the National Academy of Sciences - PNAS, 2023-01, Vol.120 (4), p.e2209964120
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Genetics (Austin), 2023-08, Vol.224 (4)
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American journal of human genetics, 2019-08, Vol.105 (2), p.413-424
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SNUPN deficiency causes a recessive muscular dystrophy due to RNA mis-splicing and ECM dysregulation
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American journal of human genetics, 2020-05, Vol.106 (5), p.717-725
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Nature communications, 2024-09, Vol.15 (1), p.7909-18, Article 7909
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Nature medicine, 2019-06, Vol.25 (6), p.911-919
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American journal of human genetics, 2020-08, Vol.107 (2), p.352-363
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- Cohen, Julie S.
- Craigen, William J.
- Cytrynbaum, Cheryl
- Ekhilevitch, Nina
- Elrick, Matthew J.
- Fatemi, Ali
- Fraser, Jamie L.
- Gallagher, Renata C.
- Guerin, Andrea
- Haynes, Devon
- High, Frances A.
- Inglese, Cara N.
- Kiss, Courtney
- Koenig, Mary Kay
- Krier, Joel
- Lindstrom, Kristin
- Marble, Michael
- Meddaugh, Hannah
- Moran, Ellen S.
- Morel, Chantal F.
- Mu, Weiyi
- Muller, Eric A.
- Nance, Jessica
- Natowicz, Marvin R.
- Numis, Adam L.
- Ostrem, Bridget
- Pappas, John
- Stafstrom, Carl E.
- Streff, Haley
- Sweetser, David A.
- Szybowska, Marta
- Walker, Melissa A.
- Wang, Wei
- Weiss, Karin
- Weksberg, Rosanna
- Wheeler, Patricia G.
- Yoon, Grace
- Kingston, Robert E.
- Juusola, Jane
2020
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