Megaconial congenital muscular dystrophy secondary to novel CHKB mutations resemble atypical Rett syndrome. (2021)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1038/s10038-021-00913-1
PubMed Identifier: 33712684
Publication URI: http://europepmc.org/abstract/MED/33712684
Type: Journal Article/Review
Volume: 66
Parent Publication: Journal of human genetics
Issue: 8
ISSN: 1434-5161