## Abstract Caveolin3 (CAV3) is a protein associated with dystrophin, dystrophin‐associated glycoproteins, and dysferlin. Mutations in the __CAV3__ gene result in certain autosomal‐dominant inherited diseases, namely, rippling muscle disease (RMD), limb‐girdle muscular dystrophy type 1C (LGMD1C), d
✦ LIBER ✦
Phenotypic variability in a Spanish family with a Caveolin-3 mutation
✍ Scribed by Paloma González-Pérez; Pía Gallano; Lidia González-Quereda; Eloy Rivas-Infante; Susana Teijeira; Carmen Navarro; Juan Bautista-Lorite
- Book ID
- 119302849
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- English
- Weight
- 316 KB
- Volume
- 276
- Category
- Article
- ISSN
- 0022-510X
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