Work

Polymicrogyria in association with hypoglycemia points to mutation in the mTOR pathway

Year: 2018

Type: article

Study design: Case Report

Source: European Journal of Medical Genetics

DOI: 10.1016/j.ejmg.2018.06.002

Authors: Chloe Stutterd, George McGillivray, Zornitza Stark, Betty Messazos, Fergus Cameron, Sue White, Ghayda Mirzaa, Richard Leventer

Institutions: Royal Children's Hospital, The University of Melbourne, Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Royal Women's Hospital, University of Washington, Seattle Children's Research Institute

Language: English

Topic: Fetal and Pediatric Neurological Disorders

Subfield: Pediatrics, Perinatology and Child Health

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2806527989

FWCI: 1.933

Cites: 15

Cited by: 19

Related to: 10