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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Detalles Bibliográficos
Autores principales: Bennett, Thomas M., Mackay, Donna S., Siegfried, Carla J., Shiels, Alan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4121231/
https://www.ncbi.nlm.nih.gov/pubmed/25090642
http://dx.doi.org/10.1371/journal.pone.0104000

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4121231/
https://www.ncbi.nlm.nih.gov/pubmed/25090642
http://dx.doi.org/10.1371/journal.pone.0104000

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