Relevance of Connexin Deafness (DFNB1) to Human Evolution **This article represents the opinions of the authors and has not been peer-reviewed.
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics
Reference37 articles.
1. Evidence for digenic inheritance of nonsyndromic hereditary hearing loss in a Swedish family;Balciuniene;Am J Hum Genet,1998
2. The conquest of deafness;Bender,1970
3. A new homonid from the Upper Miocene of Chad, Central Africa;Brunet;Nature,2002
4. The DNA revolution in population genetics;Cavalli-Sforza;Trends Genet,1998
5. Inferring nonneutral evolution from human-chimp-mouse orthologous gene trios;Clark;Science,2003
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