Mutations in the DMD gene result in two common phenotypes associated with progressive muscle weakness: the more severe Duchenne muscular dystrophy (DMD) and the milder Becker muscular dystrophy (BMD). We have previously identified a nonsense mutation (c.9G4A; p.Trp3X) within the first exon of the DM
β¦ LIBER β¦
T.P.17 Alternate translational initiation and amelioration of phenotype in the DMD gene
β Scribed by Wein, N.; Vulin, A.; Findlay, A.; Maiti, B.; Kaminoh, Y.; Taylor, L.; Flanigan, K.
- Book ID
- 119333808
- Publisher
- Elsevier Science
- Year
- 2012
- Tongue
- English
- Weight
- 64 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0960-8966
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