Correction: Megaconial congenital muscular dystrophy secondary to novel CHKB mutations resemble atypical Rett syndrome. (2021)
Attributed to:
Exosomal protein deficiencies: how abnormal RNA metabolism results in childhood-onset neurological diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1038/s10038-021-00920-2
PubMed Identifier: 33767318
Publication URI: http://europepmc.org/abstract/MED/33767318
Type: Journal Article/Review
Volume: 66
Parent Publication: Journal of human genetics
Issue: 8
ISSN: 1434-5161