The Genetic Causes of Nonsyndromic Congenital Retinal Detachment: A Genetic and Phenotypic Study of Pakistani Families

PURPOSE: To evaluate consanguineous pedigrees from Pakistan with a clinical diagnosis of nonsyndromic congenital retinal nonattachment (NCRNA) and identify genes responsible for the disease as currently only one NCRNA gene is known (atonal basic helix-loop-helix transcription factor 7: ATOH7). METHO...

Descripción completa

Detalles Bibliográficos
Autores principales: Keser, Vafa, Khan, Ayesha, Siddiqui, Sorath, Lopez, Irma, Ren, Huanan, Qamar, Raheel, Nadaf, Javad, Majewski, Jacek, Chen, Rui, Koenekoop, Robert K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2017
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5308768/
https://www.ncbi.nlm.nih.gov/pubmed/28192794
http://dx.doi.org/10.1167/iovs.16-20281

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5308768/
https://www.ncbi.nlm.nih.gov/pubmed/28192794
http://dx.doi.org/10.1167/iovs.16-20281

Ejemplares similares