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Evaluation of denaturing high-performance liquid chromatography (DHPLC) in the screening of mutations in hemophilia B patients

✍ Scribed by O. Herbert; M. Trossaërt; P. Boisseau; E. Fressinaud; F. Gerson

Book ID
109148642
Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
90 KB
Volume
2
Category
Article
ISSN
1538-7933

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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