Work

Expansion of the GRIA2 phenotypic representation: a novel de novo loss of function mutation in a case with childhood onset schizophrenia

Year: 2020

Type: article

Study design: Case Report

Source: Journal of Human Genetics

DOI: 10.1038/s10038-020-00846-1

Authors: Anna Alkelai, Shahar Shohat, Lior Greenbaum, Tanya Schechter, Benjamin Draiman, Eti Chitrit-Raveh, Shlomit Rienstein, Neha Dagaonkar, Daniel Hughes, Vimla S. Aggarwal, Erin L. Heinzen, Sagiv Shifman, David B. Goldstein, Yoav Kohn

Institutions: Columbia University Irving Medical Center, Hebrew University of Jerusalem, Tel Aviv University, Sheba Medical Center, Jerusalem Mental Health Center, University of North Carolina at Chapel Hill, Hadassah Medical Center

Language: English

Topic: Schizophrenia research and treatment

Subfield: Psychiatry and Mental health

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W3087337331

FWCI: 2.548

Cites: 23

Cited by: 26

Related to: 10