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Novel mutations in CRYGD are associated with congenital cataracts in Chinese families
Congenital cataract disease is a clinically and genetically heterogeneous lens disorder. The purpose of this study was to identify the genetic defects and to investigate the relationships between disease-causing genes and lens morphology in congenital cataracts. Patients were given a physical examin...
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| Publicado no: | Sci Rep |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4702117/ https://ncbi.nlm.nih.gov/pubmed/26732753 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep18912 |
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