The analysis of myotonia congenita mutations discloses functional clusters of amino acids within the CBS2 domain and the C-terminal peptide of the ClC-1 channel. (2018)

First Author: Altamura C

Attributed to: MICA: MRC Centre for Neuromuscular Diseases funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1002/humu.23581

PubMed Identifier: 29935101

Publication URI: http://europepmc.org/abstract/MED/29935101

Type: Journal Article/Review

Volume: 39

Parent Publication: Human mutation

Issue: 9

ISSN: 1059-7794