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Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder. (2019)

First Author: Dias CM

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