Movement disorders, 2011-08, Vol.26 (9), p.1775-1776
- Blanchard, Arnaud
- Roubertie, Agathe
- Simonetta-Moreau, Marion
- Ea, Vuthy
- Coquart, Coline
- Frederic, Melissa Y.
- Gallouedec, Gael
- Adenis, Jean-Paul
- Benatru, Isabelle
- Borg, Michel
- Burbaud, Pierre
- Calvas, Patrick
- Cif, Laura
- Damier, Philippe
- Destee, Alain
- Faivre, Laurence
- Guyant-Marechal, Lucie
- Janik, Piotr
- Janoura, Samer
- Kreisler, Alexandre
- Lusakowska, Anna
- Odent, Sylvie
- Potulska-Chromik, Anna
- Rudzińska, Monika
- Thobois, Stephane
- Vuillaume, Isabelle
- Tranchant, Christine
- Tuffery-Giraud, Sylvie
- Coubes, Philippe
- Sablonnière, Bernard
- Claustres, Mireille
- Collod-Béroud, Gwenaelle
2011
Details
- Autor(en) / Beteiligte
- Blanchard, Arnaud
- Roubertie, Agathe
- Simonetta-Moreau, Marion
- Ea, Vuthy
- Coquart, Coline
- Frederic, Melissa Y.
- Gallouedec, Gael
- Adenis, Jean-Paul
- Benatru, Isabelle
- Borg, Michel
- Burbaud, Pierre
- Calvas, Patrick
- Cif, Laura
- Damier, Philippe
- Destee, Alain
- Faivre, Laurence
- Guyant-Marechal, Lucie
- Janik, Piotr
- Janoura, Samer
- Kreisler, Alexandre
- Lusakowska, Anna
- Odent, Sylvie
- Potulska-Chromik, Anna
- Rudzińska, Monika
- Thobois, Stephane
- Vuillaume, Isabelle
- Tranchant, Christine
- Tuffery-Giraud, Sylvie
- Coubes, Philippe
- Sablonnière, Bernard
- Claustres, Mireille
- Collod-Béroud, Gwenaelle
- Titel
- Singular DYT6 phenotypes in association with new THAP1 frameshift mutations
- Ist Teil von
- Movement disorders, 2011-08, Vol.26 (9), p.1775-1776
- Ort / Verlag
- Hoboken: Wiley Subscription Services, Inc., A Wiley Company
- Erscheinungsjahr
- 2011
- Link zum Volltext
- Quelle
- Wiley Online Library - AutoHoldings Journals
- Sprache
- Englisch
- Identifikatoren
- ISSN: 0885-3185eISSN: 1531-8257DOI: 10.1002/mds.23641Titel-ID: cdi_hal_primary_oai_HAL_hal_01670065v1
- Format
- –
- Schlagworte
- Adult, Apoptosis Regulatory Proteins, Apoptosis Regulatory Proteins - genetics, Biochemistry, Molecular Biology, Biological and medical sciences, Cognitive science, Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases, DNA-Binding Proteins, DNA-Binding Proteins - genetics, Dystonia Musculorum Deformans, Dystonia Musculorum Deformans - genetics, Dystonia Musculorum Deformans - physiopathology, Female, Frameshift Mutation, Frameshift Mutation - genetics, Genetics, Human genetics, Humans, Life Sciences, Male, Medical sciences, Middle Aged, Molecular biology, Neurology, Neuroscience, Nuclear Proteins, Nuclear Proteins - genetics, Phenotype