Expanding the Phenotype and Genetic Defects Associated with the GOSR2 Gene. (2015)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1002/mdc3.12190

PubMed Identifier: 30363482

Publication URI: http://europepmc.org/abstract/MED/30363482

Type: Journal Article/Review

Volume: 2

Parent Publication: Movement disorders clinical practice

Issue: 3

ISSN: 2330-1619