Mutation update and genotype-phenotype correlations of novel and previously described mutations in TPM2 and TPM3 causing congenital myopathies. (2014)

First Author: Marttila M
Attributed to:  MICA: MRC Centre for Neuromuscular Diseases funded by MRC


No abstract provided

Bibliographic Information

Digital Object Identifier:

PubMed Identifier: 24692096

Publication URI:

Type: Journal Article/Review

Volume: 35

Parent Publication: Human mutation

Issue: 7

ISSN: 1059-7794