Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders. (2017)

First Author: Holt R

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1007/s00439-016-1745-8

PubMed Identifier: 27844144

Publication URI: http://europepmc.org/abstract/MED/27844144

Type: Journal Article/Review

Volume: 136

Parent Publication: Human genetics

Issue: 1

ISSN: 0340-6717