## Dysferlinopathies belong to the heterogeneous group of autosomal recessive muscular dystrophies. Mutations in the gene encoding dysferlin (DYSF) lead to distinct phenotypes, mainly Limb Girdle Muscular Dystrophy type 2B (LGMD2B) and Miyoshi myopathy (MM). Here, we analysed the mutational data fr
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Array-CGH analysis of a cohort of 86 patients with oculoauriculovertebral spectrum
✍ Scribed by Caroline Rooryck; Noui Souakri; Dorothée Cailley; Julie Bouron; Cyril Goizet; Marie-Ange Delrue; Sandrine Marlin; Feclad Didier Lacombe; Benoît Arveiler
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 95 KB
- Volume
- 152A
- Category
- Article
- ISSN
- 1552-4825
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