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Connexin mutations in hearing loss, dermatological and neurological disorders

✍ Scribed by Raquel Rabionet; Núria López-Bigas; Maria Lourdes Arbonès; Xavier Estivill

Book ID
117787947
Publisher
Elsevier Science
Year
2002
Tongue
English
Weight
968 KB
Volume
8
Category
Article
ISSN
1471-4914

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## Abstract The connexins are a family of proteins whose major function is as part of the gap junctions of cell‐to‐cell channels. They are expressed in several tissues including brain, skin, and cochlea. Mutations in connexin genes play a major role in non‐syndromic sensorineural deafness, but have