Targeted high-throughput sequencing identifies mutations in atlastin-1 as a cause of hereditary sensory neuropathy type I. (2011)

First Author: Guelly C

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2010.12.003

PubMed Identifier: 21194679

Publication URI: http://europepmc.org/abstract/MED/21194679

Type: Journal Article/Review

Volume: 88

Parent Publication: American journal of human genetics

Issue: 1

ISSN: 0002-9297