Connexinopathies: a structural and functional glimpse

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 Tooth disease (Cx32), occulodentodigital dysplasia and cardiopathies (Cx43), and cataracts (Cx46, C...

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Detalles Bibliográficos
Publicado en:BMC Cell Biol
Main Authors: García, Isaac E., Prado, Pavel, Pupo, Amaury, Jara, Oscar, Rojas-Gómez, Diana, Mujica, Paula, Flores-Muñoz, Carolina, González-Casanova, Jorge, Soto-Riveros, Carolina, Pinto, Bernardo I., Retamal, Mauricio A., González, Carlos, Martínez, Agustín D.
Formato: Artigo
Idioma:Inglês
Publicado: BioMed Central 2016
Assuntos:
Review
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4896260/
https://ncbi.nlm.nih.gov/pubmed/27228968
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12860-016-0092-x
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