Mutation update and genotype-phenotype correlations of novel and previously described mutations in TPM2 and TPM3 causing congenital myopathies. (2014)
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.22554
PubMed Identifier: 24692096
Publication URI: http://europepmc.org/abstract/MED/24692096
Type: Journal Article/Review
Volume: 35
Parent Publication: Human mutation
Issue: 7
ISSN: 1059-7794