Characterising a homozygous two-exon deletion in UQCRH: comparing human and mouse phenotypes. (2021)
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/10.15252/emmm.202114397
PubMed Identifier: 34750991
Publication URI: http://europepmc.org/abstract/MED/34750991
Type: Journal Article/Review
Volume: 13
Parent Publication: EMBO molecular medicine
Issue: 12
ISSN: 1757-4676