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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4636350/
https://www.ncbi.nlm.nih.gov/pubmed/26628857

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4636350/
https://www.ncbi.nlm.nih.gov/pubmed/26628857

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