Mapping of a new locus associated with autosomal recessive congenital cataract to chromosome 3q

PURPOSE: To localize the disease interval for autosomal recessive congenital cataracts in a consanguineous Pakistani family. METHODS: All affected individuals underwent detailed ophthalmologic examination. Blood samples were collected and genomic DNA was extracted. A genome-wide scan was performed w...

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Hoofdauteurs: Sabir, Namerah, Riazuddin, S. Amer, Butt, Tariq, Iqbal, Farheena, Nasir, Idrees A., Zafar, Ahmad U., Qazi, Zaheeruddin A., Butt, Nadeem H., Khan, Shaheen N., Husnain, Tayyab, Hejtmancik, J. Fielding, Riazuddin, Sheikh
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Molecular Vision 2010
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Research Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3002966/
https://ncbi.nlm.nih.gov/pubmed/21179239
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