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Large novel deletions detected in Chinese families with aniridia: correlation between genotype and phenotype

PURPOSE: To describe the clinical and genetic findings in two Chinese families with aniridia and other ocular abnormalities. METHODS: Two unrelated families were examined clinically. After informed consent was obtained, genomic DNA was extracted from the venous blood of all participants. Mutation sc...

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Autors principals: Zhang, Xiaohui, Zhang, Qingsheng, Tong, Yi, Dai, Hanjun, Zhao, Xin, Bai, Fengge, Xu, Liang, Li, Yang
Format: Artigo
Idioma:Inglês
Publicat: Molecular Vision 2011
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3044699/
https://ncbi.nlm.nih.gov/pubmed/21364908
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