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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Veröffentlicht in:Mol Vis
Hauptverfasser: 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
Format: Artigo
Sprache:Inglês
Veröffentlicht: Molecular Vision 2015
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Research Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4636350/
https://ncbi.nlm.nih.gov/pubmed/26628857
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