Not to Miss: Intronic Variants, Treatment, and Review of the Phenotypic Spectrum in VPS13D-Related Disorder. (2023)
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/10.3390/ijms24031874
PubMed Identifier: 36768210
Publication URI: http://europepmc.org/abstract/MED/36768210
Type: Journal Article/Review
Volume: 24
Parent Publication: International journal of molecular sciences
Issue: 3
ISSN: 1422-0067