A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy
- Author
- LEMMERS, Richard J. L. F1 ; VAN DER VLIET, Patrick J1 ; MILLER, Daniel G8 ; TAPSCOTT, Stephen J6 ; TAWIL, Rabi9 ; FRANTS, Rune R1 ; VAN DER MAAREL, Silvère M1 ; KLOOSTER, Rinse1 ; SACCONI, Sabrina2 ; CAMANO, Pilar3 4 ; DAUWERSE, Johannes G5 ; SNIDER, Lauren6 ; STRAASHEIJM, Kirsten R1 ; VAN OMMEN, Gert Jan1 ; PADBERG, George W7
[1] Department of Human Genetics, Leiden University Medical Center, 2333 ZA Leiden, Netherlands
[2] Centre de Reference pour les Maladies Neuromusculaires and CNRS UMR6543, Nice University, 06202 Nice, France
[3] Department of Neurosciences, BioDonostia Health Research Institute, Hospital Donostia, 20014 San Sebastián, Spain
[4] CIBERNED, Instituto de Salud Carlos III, 28029 Madrid, Spain
[5] Department of Clinical Genetics, Leiden University Medical Center, 2333 ZA Leiden, Netherlands
[6] Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, United States
[7] Department of Neurology, Radboud University Medical Center Nijmegen, 6500 HC Nijmegen, Netherlands
[8] Department of Pediatrics, University of Washington, Seattle, WA 98195, United States
[9] Department of Neurology, University of Rochester Medical Center, Rochester, NY 14642, United States - Source
Science (Washington, D.C.). 2010, Vol 329, Num 5999, pp 1650-1653, 4 p
- CODEN
- SCIEAS
- ISSN
- 0036-8075
- Scientific domain
- Multidisciplinary
- Publisher
- American Association for the Advancement of Science, Washington, DC
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Dystrophie musculaire Déterminisme génétique Facioscapulohuméral Homme Polymorphisme Maladie héréditaire Pathologie du système nerveux Pathologie neuromusculaire
- Keyword (en)
- Muscular dystrophy Genetic determinism Facioscapulohumeral Human Polymorphism Genetic disease Nervous system diseases Neuromuscular diseases
- Keyword (es)
- Distrofia muscular Determinismo genético Facioescapulohumeral Hombre Polimorfismo Enfermedad hereditaria Sistema nervioso patología Neuromuscular patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17H Diseases of striated muscles. Neuromuscular diseases
- Discipline
- Neurology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 23264922
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1126/science.1189044 
https://dx.doi.org/10.1126/science.1189044
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