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


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Bibliographic Information

Digital Object Identifier:

PubMed Identifier: 29935101

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Type: Journal Article/Review

Volume: 39

Parent Publication: Human mutation

Issue: 9

ISSN: 1059-7794