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
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4896260/
https://www.ncbi.nlm.nih.gov/pubmed/27228968
http://dx.doi.org/10.1186/s12860-016-0092-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4896260/
https://www.ncbi.nlm.nih.gov/pubmed/27228968
http://dx.doi.org/10.1186/s12860-016-0092-x

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