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Identification and characterization of six β‐crystallin gene mutations associated with congenital cataract in Chinese families
BACKGROUND: This study aims to identify the underlying genetic defects of β‐crystallin (CRYB) genes responsible for congenital cataracts in a group of Chinese families. METHODS: Detailed family history and clinical data of six Chinese families with autosomal dominant congenital cataracts were record...
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| Publicado no: | Mol Genet Genomic Med |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8104166/ https://ncbi.nlm.nih.gov/pubmed/33594837 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.1617 |
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