Behr syndrome and hypertrophic cardiomyopathy in a family with a novel UCHL1 deletion. (2020)
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/10.1007/s00415-020-10059-3
PubMed Identifier: 32656641
Publication URI: http://europepmc.org/abstract/MED/32656641
Type: Journal Article/Review
Volume: 267
Parent Publication: Journal of neurology
Issue: 12
ISSN: 0340-5354