## Communicated by Jürgen Horst Sarcoglycanopathies, affecting the dystrophin-associated sarcoglycan (SG) complex, are a heterogeneous group of neuromuscular disorders. A subgroup of these disorders, limb-girdle muscular dystrophy type 2C (LGMD2C) is an autosomal recessive disorder, clinically man
✦ LIBER ✦
C283Y mutation and other C-terminal nucleotide changes in the γ-sarcoglycan gene in the Bulgarian Gypsy population
✍ Scribed by Albena Todorova; Angel Ashikov; Olga Beltcheva; Ivailo Tournev; Ivo Kremensky
- Book ID
- 101263997
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 60 KB
- Volume
- 15
- Category
- Article
- ISSN
- 1059-7794
No coin nor oath required. For personal study only.
✦ Synopsis
The authors wish to correct a mistake in the amino acid change stemming from a 490C>T nucleotide change. In this article, the nucleotide change is stated to lead to a Q165X amino acid change. The 490C>T nucleotide change should actually cause a Q164X amino acid change.
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