## Communicated by Christopher G. Mathew The availability of the complete sequence of the human genome has dramatically facilitated the search for disease-causing sequence variations. In fact, the rate-limiting step has shifted from the discovery and characterization of candidate genes to the actu
✦ LIBER ✦
Screening for mutations in candidate genes for hypospadias
✍ Scribed by Nordenskjöld, Agenta ;Friedman, Eitan ;Tappar-Persson, Margareta ;Söderhäll, Cilla ;Leviav, Amos ;Svensson, Jan ;Anvret, Maria
- Publisher
- Springer
- Year
- 1999
- Tongue
- English
- Weight
- 636 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0300-5623
No coin nor oath required. For personal study only.
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## 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
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