Identification and characterization of novel MPC1 gene variants causing mitochondrial pyruvate carrier deficiency. (2022)
Attributed to:
MRC Strategic Award to establish an International Centre for Genomic Medicine in Neuromuscular Diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1002/jimd.12462
PubMed Identifier: 34873722
Publication URI: http://europepmc.org/abstract/MED/34873722
Type: Journal Article/Review
Volume: 45
Parent Publication: Journal of inherited metabolic disease
Issue: 2
ISSN: 0141-8955