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Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndrome. (2014)

First Author: Thomas AC

Attributed to: Using Next Generation Sequencing to Unravel the Pathogenesis of Sporadic Inclusion Body Myositis - The International IBM Consortium Genetic Study funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2014.10.007

PubMed Identifier: 25439728

Publication URI: http://europepmc.org/abstract/MED/25439728

Type: Journal Article/Review

Volume: 95

Parent Publication: American journal of human genetics

Issue: 5

ISSN: 0002-9297