Mutations in the GlyT2 gene (SLC6A5) are a second major cause of startle disease. (2012)

First Author: Carta E

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1074/jbc.M112.372094

PubMed Identifier: 22700964

Publication URI: http://europepmc.org/abstract/MED/22700964

Type: Journal Article/Review

Volume: 287

Parent Publication: The Journal of biological chemistry

Issue: 34

ISSN: 0021-9258