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

Rad, A (2019) Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder. American journal of human genetics.

Full text not available from this repository.
Item Type: Article
Subjects: R Medicine > R Medicine (General)
Depositing User: Saeed Shoja
Date Deposited: 23 Dec 2019 10:35
Last Modified: 23 Dec 2019 10:35
URI: http://eprints.medsab.ac.ir/id/eprint/1340

Actions (login required)

View Item View Item