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Mutational analysis of CYP2C8 in hypertensive patients using denaturing high performance liquid chromatography

✍ Scribed by L. K. Teh; M. K. Zahri; Z. A. Zakaria; R. Ismail; M. Z. Salleh


Book ID
108849343
Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
163 KB
Volume
35
Category
Article
ISSN
0269-4727

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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