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Further evidence for P59L mutation in GJA3 associated with autosomal dominant congenital cataract
CONTEXT: Congenital cataracts are one of the common eye disorders leading to visual impairment or blindness in children worldwide. We found a Chinese family with autosomal dominant pulverulent cataract. AIMS: To identify the pathogenic gene mutation in a Chinese family with autosomal dominant inheri...
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| Publicado no: | Indian J Ophthalmol |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5026076/ https://ncbi.nlm.nih.gov/pubmed/27609163 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0301-4738.190139 |
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