Bi-allelic mutations in MYL1 cause a severe congenital myopathy. (2018)
Attributed to:
MICA: MRC Centre for Neuromuscular Diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddy320
PubMed Identifier: 30215711
Publication URI: http://europepmc.org/abstract/MED/30215711
Type: Journal Article/Review
Volume: 27
Parent Publication: Human molecular genetics
Issue: 24
ISSN: 0964-6906