📣 Try out the NEW Gateway to Research and let us know what you think.

We're looking for users to test the new service during August and September and share their feedback. Express your interest by completing this short form.

Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII a1 Chain. (2015)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2015.10.017

PubMed Identifier: 26626625

Publication URI: http://europepmc.org/abstract/MED/26626625

Type: Journal Article/Review

Volume: 97

Parent Publication: American journal of human genetics

Issue: 6

ISSN: 0002-9297