## Abstract __KCNK6__ encodes a tandem pore domain potassium channel, TWIK‐2, that maps to chromosome 19. Both STS and linkage maps established __KCNK6__ as a positional candidate gene for DFNA4, a form of autosomal dominant nonsyndromic hereditary hearing loss. Identification and characterization
Genomic organization and mutation analysis of three candidate genes for hereditary neuralgic amyotrophy
✍ Scribed by Gert Hünermund; Anja Schirmacher; Bernd Ringelstein; Peter Young; Giles D. Watts; Jan Meuleman; Eva Nelis; Phillip F. Chance; Vincent Timmerman; Florian Stögbauer; Gregor Kuhlenbäumer
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 75 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0148-639X
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