Mutations in CPAMD8 Cause a Unique Form of Autosomal-Recessive Anterior Segment Dysgenesis. (2016)

First Author: Cheong SS
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/10.1016/j.ajhg.2016.09.022

PubMed Identifier: 27839872

Publication URI: http://europepmc.org/abstract/MED/27839872

Type: Journal Article/Review

Volume: 99

Parent Publication: American journal of human genetics

Issue: 6

ISSN: 0002-9297