Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease. (2006)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/ng1814

PubMed Identifier: 16751771

Publication URI: http://europepmc.org/abstract/MED/16751771

Type: Journal Article/Review

Volume: 38

Parent Publication: Nature genetics

Issue: 7

ISSN: 1061-4036