Mutation Screening in the miR-183/96/182 Cluster in Patients With Inherited Retinal Dystrophy

Inherited retinal dystrophy (IRD) is a heterogenous blinding eye disease and affects more than 200,000 Americans and millions worldwide. By far, 270 protein-coding genes have been identified to cause IRD when defective. However, only one microRNA (miRNA), miR-204, has been reported to be responsible...

Descripción completa

Detalles Bibliográficos
Autores principales: Xu, Shunbin, Coku, Ardian, Muraleedharan, Chithra K., Harajli, Ali, Mishulin, Eric, Dahabra, Chafic, Choi, Joanne, Garcia, William J., Webb, Kaylie, Birch, David, Goetz, Kerry, Li, Weifeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7785829/
https://www.ncbi.nlm.nih.gov/pubmed/33425925
http://dx.doi.org/10.3389/fcell.2020.619641

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7785829/
https://www.ncbi.nlm.nih.gov/pubmed/33425925
http://dx.doi.org/10.3389/fcell.2020.619641

Ejemplares similares