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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Detalhes bibliográficos
Publicado no: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
Formato: Artigo
Idioma:Inglês
Publicado em: Molecular Vision 2015
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Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4636350/
https://ncbi.nlm.nih.gov/pubmed/26628857
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