Connexinopathies: a structural and functional glimpse

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Connexinopathies a structural and functional glimpse.pdf (1.33 MB)

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2016

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Article

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Artículos Medicina y Ciencias de la Salud

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http://dx.doi.org/10.1186/s12860-016-0092-x
 http://hdl.handle.net/11447/5300

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Abstract

Mutations in human connexin (Cx) genes have been related to diseases, which we termed connexinopathies. Such hereditary disorders include nonsyndromic or syndromic deafness (Cx26, Cx30), Charcot Marie...

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Citation

García IE, Prado P, Pupo A, Jara O, Rojas-Gómez D, Mujica P, Flores-Muñoz C, González-Casanova J, Soto-Riveros C, Pinto BI, Retamal MA, González C, Martínez AD. Connexinopathies: a structural and functional glimpse. BMC Cell Biol. 2016 May 24;17 Suppl 1(Suppl 1):17

Keywords

Connexins , Hemichannels , Gap junction channels , Sstructure and function , Human genetic disease

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