Assembly of the cochlear gap junction macromolecular complex requires connexin 26

Hereditary deafness affects approximately 1 in 2,000 children. Mutations in the gene encoding the cochlear gap junction protein connexin 26 (CX26) cause prelingual, nonsyndromic deafness and are responsible for as many as 50% of hereditary deafness cases in certain populations. Connexin-associated d...

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Autors principals: Kamiya, Kazusaku, Yum, Sabrina W., Kurebayashi, Nagomi, Muraki, Miho, Ogawa, Kana, Karasawa, Keiko, Miwa, Asuka, Guo, Xueshui, Gotoh, Satoru, Sugitani, Yoshinobu, Yamanaka, Hitomi, Ito-Kawashima, Shioko, Iizuka, Takashi, Sakurai, Takashi, Noda, Tetsuo, Minowa, Osamu, Ikeda, Katsuhisa
Format: Artigo
Idioma:Inglês
Publicat: American Society for Clinical Investigation 2014
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3973107/
https://ncbi.nlm.nih.gov/pubmed/24590285
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI67621
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