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A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani family
PURPOSE: The purpose of this study was to identify the underlying molecular genetic defect in a large consanguineous Pakistani family with Oguchi disease who had been given a diagnosis of autosomal recessive retinitis pigmentosa. METHODS: The family was genotyped with the Affymetrix 10K single nucle...
Autores principales: | Azam, Maleeha, Collin, Rob W.J., Khan, Muhammad Imran, Shah, Syed Tahir Abbas, Qureshi, Nadeem, Ajmal, Muhammad, den Hollander, Anneke I., Qamar, Raheel, Cremers, Frans P.M. |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Molecular Vision
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2742643/ https://www.ncbi.nlm.nih.gov/pubmed/19753316 |
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