Biallelic and monoallelic variants in PLXNA1 are implicated in a novel neurodevelopmental disorder with variable cerebral and eye anomalies. (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/10.1038/s41436-021-01196-9
PubMed Identifier: 34054129
Publication URI: http://europepmc.org/abstract/MED/34054129
Type: Journal Article/Review
Volume: 23
Parent Publication: Genetics in medicine : official journal of the American College of Medical Genetics
Issue: 9
ISSN: 1098-3600