Hereditary sensory and autonomic neuropathy type 1 (HSANI) caused by a novel mutation in SPTLC2. (2013)

First Author: Murphy SM

Attributed to: MICA: MRC Centre for Neuromuscular Diseases funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1212/wnl.0b013e318295d789

PubMed Identifier: 23658386

Publication URI: http://europepmc.org/abstract/MED/23658386

Type: Journal Article/Review

Volume: 80

Parent Publication: Neurology

Issue: 23

ISSN: 0028-3878