Multifunctional ion transport properties of human SLC4A11: comparison of the SLC4A11-B and SLC4A11-C variants

Congenital hereditary endothelial dystrophy (CHED), Harboyan syndrome (CHED with progressive sensorineural deafness), and potentially a subset of individuals with late-onset Fuchs' endothelial corneal dystrophy are caused by mutations in the SLC4A11 gene that results in corneal endothelial cell...

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Detalhes bibliográficos
Publicado no:Am J Physiol Cell Physiol
Main Authors: Kao, Liyo, Azimov, Rustam, Shao, Xuesi M., Frausto, Ricardo F., Abuladze, Natalia, Newman, Debra, Aldave, Anthony J., Kurtz, Ira
Formato: Artigo
Idioma:Inglês
Publicado em: American Physiological Society 2016
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5130583/
https://ncbi.nlm.nih.gov/pubmed/27581649
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajpcell.00233.2016
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