Functional analysis of FOXE3 mutations causing dominant and recessive ocular anterior segment disease. (2015)

First Author: Islam L
Attributed to:  MRC Wellcome Trust Human Developmental Biology Resource (HDBR) funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1002/humu.22741

PubMed Identifier: 25504734

Publication URI: http://europepmc.org/abstract/MED/25504734

Type: Journal Article/Review

Volume: 36

Parent Publication: Human mutation

Issue: 3

ISSN: 1059-7794