Denaturing High Performance Liquid Chromatography Detection of SDHB, SDHD, and VHL Germline Mutations in Pheochromocytoma
β Scribed by Goswin Y. Meyer-Rochow; Janine M. Smith; Anne-Louise Richardson; Deborah J. Marsh; Stan B. Sidhu; Bruce G. Robinson; Diana E. Benn
- Book ID
- 116704505
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- English
- Weight
- 232 KB
- Volume
- 157
- Category
- Article
- ISSN
- 0022-4804
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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