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A missense mutation in CRYBA4 associated with congenital cataract and microcornea
PURPOSE: To identify mutations in a Chinese family with congenital cataract and microcornea. METHODS: Detailed family history and clinical data were recorded. Genomic DNA was extracted from leukocytes of venous blood of the patients and noncarriers in this family along with 100 normal individuals. A...
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| Autori principali: | , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Molecular Vision
2010
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2890555/ https://ncbi.nlm.nih.gov/pubmed/20577656 |
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