Hexosamine biosynthetic pathway mutations cause neuromuscular transmission defect. (2011)

First Author: Senderek J

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2011.01.008

PubMed Identifier: 21310273

Publication URI: http://europepmc.org/abstract/MED/21310273

Type: Journal Article/Review

Volume: 88

Parent Publication: American journal of human genetics

Issue: 2

ISSN: 0002-9297