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Mutations in GRM6 identified in consanguineous Pakistani families with congenital stationary night blindness

PURPOSE: This study was undertaken to investigate the causal mutations responsible for autosomal recessive congenital stationary night blindness (CSNB) in consanguineous Pakistani families. METHODS: Two consanguineous families with multiple individuals manifesting symptoms of stationary night blindn...

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發表在:Mol Vis
Main Authors: Naeem, Muhammad Asif, Gottsch, Alexander D. H., Ullah, Inayat, Khan, Shaheen N., Husnain, Tayyab, Butt, Nadeem H., Qazi, Zaheeruddin A., Akram, Javed, Riazuddin, Sheikh, Ayyagari, Radha, Hejtmancik, J. Fielding, Riazuddin, S. Amer
格式: Artigo
語言:Inglês
出版: Molecular Vision 2015
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC4636350/
https://ncbi.nlm.nih.gov/pubmed/26628857
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