GJB2 mutations and additional disabilities in a pediatric cochlear implant population
โ Scribed by S. Wiley; D. Choo; J. Meinzen-Derr; L. Hilbert; J. Greinwald
- Book ID
- 116564068
- Publisher
- Elsevier Science
- Year
- 2006
- Tongue
- English
- Weight
- 175 KB
- Volume
- 70
- Category
- Article
- ISSN
- 0165-5876
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Mutations in the gene of the gap junction protein Connexin 31 (CX31; other connexin 1 Laboratory of Molecular genes abbreviated by CX+#, i.e. Connexin 30 = CX30) have been demonstrated to be Otology, Epstein Laboratories, responsible for both autosomal dominant and recessive nonsyndromic hereditary