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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Detalles Bibliográficos
Autores principales: 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
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002966/
https://www.ncbi.nlm.nih.gov/pubmed/21179239

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002966/
https://www.ncbi.nlm.nih.gov/pubmed/21179239

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