Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesis. (2011)

First Author: Mill P
Attributed to:  Genetic models of human disease funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2011.03.015

PubMed Identifier: 21473986

Publication URI: http://europepmc.org/abstract/MED/21473986

Type: Journal Article/Review

Volume: 88

Parent Publication: American journal of human genetics

Issue: 4

ISSN: 0002-9297