Biallelic Loss-of-Function NDUFA12 Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh-Like Syndrome to Isolated Optic Atrophy. (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/mdc3.13398
PubMed Identifier: 35141356
Publication URI: http://europepmc.org/abstract/MED/35141356
Type: Journal Article/Review
Volume: 9
Parent Publication: Movement disorders clinical practice
Issue: 2
ISSN: 2330-1619