Consolidating biallelic SDHD variants as a cause of mitochondrial complex II deficiency. (2021)
Attributed to:
Promoting Innovation and Collaboration: Translational Medicine in Exeter 2 (PICTME2)
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1038/s41431-021-00887-w
PubMed Identifier: 34012134
Publication URI: http://europepmc.org/abstract/MED/34012134
Type: Journal Article/Review
Volume: 29
Parent Publication: European journal of human genetics : EJHG
Issue: 10
ISSN: 1018-4813