Deep geno- and phenotyping in two consanguineous families with CMT2 reveals HADHA as an unusual disease-causing gene and an intronic variant in GDAP1 as an unusual mutation. (2021)
Attributed to:
Understanding the genes for Parkinson's disease
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1007/s00415-020-10171-4
PubMed Identifier: 32897397
Publication URI: http://europepmc.org/abstract/MED/32897397
Type: Journal Article/Review
Volume: 268
Parent Publication: Journal of neurology
Issue: 2
ISSN: 0340-5354