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Mutations in CSPP1, encoding a core centrosomal protein, cause a range of ciliopathy phenotypes in humans. (2014)

First Author: Shaheen R

Attributed to: Ciliopathy disease gene identification by whole exome medical resequencing funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2013.11.010

PubMed Identifier: 24360803

Publication URI: http://europepmc.org/abstract/MED/24360803

Type: Journal Article/Review

Volume: 94

Parent Publication: American journal of human genetics

Issue: 1

ISSN: 0002-9297