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Relevance of Connexin Deafness (DFNB1) to Human Evolution

✍ Scribed by Walter E. Nance; Michael J. Kearsey

Book ID
117854441
Publisher
American Society of Human Genetics
Year
2004
Tongue
English
Weight
333 KB
Volume
74
Category
Article
ISSN
0002-9297

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## Communicated by Henrik Dahl Mutations in the DFNB1 locus, where two connexin genes are located (GJB2 and GJB6), account for half of congenital cases of nonsyndromic autosomal recessive deafness. Because of the high frequency of DFNB1 gene mutations and the availability of genetic diagnostic tes