‘RetinoGenetics’: a comprehensive mutation database for genes related to inherited retinal degeneration

Mostrar otras versiones (1)

Inherited retinal degeneration (IRD), a leading cause of human blindness worldwide, is exceptionally heterogeneous with clinical heterogeneity and genetic variety. During the past decades, tremendous efforts have been made to explore the complex heterogeneity, and massive mutations have been identif...

Descripción completa

Detalles Bibliográficos
Autores principales: Ran, Xia, Cai, Wei-Jun, Huang, Xiu-Feng, Liu, Qi, Lu, Fan, Qu, Jia, Wu, Jinyu, Jin, Zi-Bing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Database Tool
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4060621/
https://www.ncbi.nlm.nih.gov/pubmed/24939193
http://dx.doi.org/10.1093/database/bau047

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4060621/
https://www.ncbi.nlm.nih.gov/pubmed/24939193
http://dx.doi.org/10.1093/database/bau047

Ejemplares similares