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Detection of genetic mutations in Barrett's esophagus using denaturing high pressure liquid chromatography (DHPLC)

✍ Scribed by Kausilia K. Krishnadathl; Ken Taniguchi; Navtej S. Buttar; Marlys A. Anderson; Lori S. Lutzke; Wanguo Liu; Chiping Qian; Ping Yang; David I. Smith; Kenneth K. Wang


Book ID
119426090
Publisher
Elsevier Science
Year
2000
Tongue
English
Weight
187 KB
Volume
118
Category
Article
ISSN
0016-5085

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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