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...
Kaydedildi:
| Asıl Yazarlar: | , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Public Library of Science (PLoS)
2014-01-01
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| Seri Bilgileri: | PLoS ONE |
| Online Erişim: | https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/25090642/?tool=EBI |
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