A dominant mutation in MAPKAPK3, an actor of p38 signaling pathway, causes a new retinal dystrophy involving Bruch's membrane and retinal pigment epithelium.

Details

Language :

English

ISSN :

09646906

Volume :

25

Issue :

5

Database :

Complementary Index

Journal :

Human Molecular Genetics

Publication Type :

Academic Journal

Accession number :

113397224

Full Text :

https://doi.org/10.1093/hmg/ddv624