Assessment of denaturing high-performanc
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Doris Lin; Jayne A. Goldstein; Anand N. Mhatre; Lawrence R. Lustig; Markus Pfist
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Article
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2001
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John Wiley and Sons
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English
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## Communicated by Mark H. Paalman Mutations in the gene GJB2 encoding connexin 26 (Cx26), a gap junction protein, have been shown to be responsible for a majority of recessive nonsyndromic hereditary hearing impairment in children. Over 60 different mutations in Cx26 have been reported. To obviat