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Studies related to innovations in cochlear implants

✍ Scribed by Alan J Lupin


Book ID
117551918
Publisher
Elsevier Science
Year
2003
Tongue
English
Weight
197 KB
Volume
1254
Category
Article
ISSN
0531-5131

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Molecular study in Brazilian cochlear im
✍ Thalita Vitachi Christiani; Fabiana Alexandrino; Camila AndrΓ©a de Oliveira; Regi πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons 🌐 English βš– 74 KB

## Abstract The most common form of non‐syndromic autosomal recessive deafness (NSRD) is caused by mutations in the __GJB2__ gene. Recently, a deletion truncating the __GJB6__ gene, called del(__GJB6‐__D13S1830) has also been described normally accompanying mutations in another allele of the __GJB2