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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Medknow Publications & Media Pvt Ltd
2016
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5026076/ https://www.ncbi.nlm.nih.gov/pubmed/27609163 http://dx.doi.org/10.4103/0301-4738.190139 |