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C283Y gamma-sarcoglycan gene mutation in the Bulgarian Roma (Gypsy) population: prevalence study and carrier screening in a high-risk community

✍ Scribed by B Georgieva; A Todorova; I Tournev; V Mitev; I Kremensky

Book ID: 110887949
Publisher: John Wiley and Sons
Year: 2004
Tongue: English
Weight: 405 KB
Volume: 66
Category: Article
ISSN: 0009-9163
DOI: 10.1111/j.1399-0004.2004.00335.x

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## 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

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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.