Molecular characterization of retinitis pigmentosa in Saudi Arabia

PURPOSE: To catalog mutations that underlie retinitis pigmentosa (RP) in Saudi Arabia using a representative sample. METHODS: Fifty-two patients with RP were recruited and their homozygosity mapping, with or without linkage analysis, was used to suggest the causative genes followed by bidirectional...

Descripción completa

Detalles Bibliográficos
Autores principales: Aldahmesh, Mohammed A., Abu Safieh, Leen, Alkuraya, Hisham, Al-Rajhi, Ali, Shamseldin, Hanan, Hashem, Mais, Alzahrani, Fatemah, Khan, Arif O., Alqahtani, Faisal, Rahbeeni, Zuhair, Alowain, Mohammed, Khalak, Hanif, Al-Hazzaa, Salwa, Meyer, Brian F., Alkuraya, Fowzan S.
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2009
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786884/
https://www.ncbi.nlm.nih.gov/pubmed/19956407

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786884/
https://www.ncbi.nlm.nih.gov/pubmed/19956407

Ejemplares similares