Confirmation of the Role of DHX38 in the Etiology of Early-Onset Retinitis Pigmentosa

PURPOSE: Retinitis pigmentosa (RP) is a genetically heterogeneous trait with autosomal-recessive (ar) inheritance underlying 50% of genetic disease cases. Sixty-one arRP genes have been identified, and recently, DHX38 has been reported as a potential candidate gene for arRP with only a single family...

Descripción completa

Detalles Bibliográficos
Autores principales: Latif, Zahid, Chakchouk, Imen, Schrauwen, Isabelle, Lee, Kwanghyuk, Santos-Cortez, Regie Lyn P., Abbe, Izoduwa, Acharya, Anushree, Jarral, Afeefa, Ali, Imran, Ullah, Ehsan, Khan, Muhammad Nasim, Ali, Ghazanfar, Tahir, Tufail Hussain, Bamshad, Michael J., Nickerson, Deborah A., Ahmad, Wasim, Ansar, Muhammad, Leal, Suzanne M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2018
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6133250/
https://www.ncbi.nlm.nih.gov/pubmed/30208423
http://dx.doi.org/10.1167/iovs.18-23849

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6133250/
https://www.ncbi.nlm.nih.gov/pubmed/30208423
http://dx.doi.org/10.1167/iovs.18-23849

Ejemplares similares