Stargardt macular dystrophy: common ABCA4 mutations in South Africa—establishment of a rapid genetic test and relating risk to patients

PURPOSE: Based on the previous indications of founder ATP-binding cassette sub-family A member 4 gene (ABCA4) mutations in a South African subpopulation, the purpose was to devise a mechanism for identifying common disease-causing mutations in subjects with ABCA4-associated retinopathies (AARs). Fac...

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Detalles Bibliográficos
Autores principales: Roberts, Lisa J., Nossek, Christel A., Greenberg, L. Jacquie, Ramesar, Rajkumar S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275638/
https://www.ncbi.nlm.nih.gov/pubmed/22328824

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275638/
https://www.ncbi.nlm.nih.gov/pubmed/22328824

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