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Mutation of the Melastatin-Related Cation Channel, TRPM3, Underlies Inherited Cataract and Glaucoma

Inherited forms of cataract are a clinically important and genetically heterogeneous cause of visual impairment that usually present at an early age with or without systemic and/or other ocular abnormalities. Here we have identified a new locus for inherited cataract and high-tension glaucoma with v...

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Detalhes bibliográficos
Main Authors: Bennett, Thomas M., Mackay, Donna S., Siegfried, Carla J., Shiels, Alan
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4121231/
https://ncbi.nlm.nih.gov/pubmed/25090642
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0104000
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