Mutations in FYCO1 Cause Autosomal-Recessive Congenital Cataracts

Congenital cataracts (CCs), responsible for about one-third of blindness in infants, are a major cause of vision loss in children worldwide. Autosomal-recessive congenital cataracts (arCC) form a clinically diverse and genetically heterogeneous group of disorders of the crystalline lens. To identify...

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Hlavní autoři: Chen, Jianjun, Ma, Zhiwei, Jiao, Xiaodong, Fariss, Robert, Kantorow, Wanda Lee, Kantorow, Marc, Pras, Eran, Frydman, Moshe, Pras, Elon, Riazuddin, Sheikh, Riazuddin, S. Amer, Hejtmancik, J. Fielding
Médium: Artigo
Jazyk:Inglês
Vydáno: Elsevier 2011
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3113247/
https://ncbi.nlm.nih.gov/pubmed/21636066
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2011.05.008
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