Mutation of POC1B in a severe syndromic retinal ciliopathy. (2014)

First Author: Beck BB

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1002/humu.22618

PubMed Identifier: 25044745

Publication URI: http://europepmc.org/abstract/MED/25044745

Type: Journal Article/Review

Volume: 35

Parent Publication: Human mutation

Issue: 10

ISSN: 1059-7794