Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder. (2019)
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/10.1016/j.ajhg.2019.09.025
PubMed Identifier: 31668703
Publication URI: http://europepmc.org/abstract/MED/31668703
Type: Journal Article/Review
Volume: 105
Parent Publication: American journal of human genetics
Issue: 5
ISSN: 0002-9297