Connexin26 deafness in several interconnected families

Mutations in the connexin26 gene are the basis of much autosomal recessive sensorineural deafness. There is a high frequency of mutant alleles, largely accounted for by one common mutation, 35delG. We have studied a group of families, who had been brought together through marriages between Deaf pers...

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Bibliografiske detaljer
Main Authors: Wilcox, S., Osborn, A., Allen-Powell, D., Maw, M., Dahl, H., Gardner, R
Format: Artigo
Sprog:Inglês
Udgivet: BMJ Group 1999
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Original Articles
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1734366/
https://ncbi.nlm.nih.gov/pubmed/10353784
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