Work

Epigenomic variations manifesting as a loss of heterozygosity affecting imprinted genes represent a molecular mechanism of autism spectrum disorders and intellectual disability in children

Year: 2019

Type: article

Study design: Observational Study

Source: S S Korsakov Journal of Neurology and Psychiatry

DOI: 10.17116/jnevro201911905191

Authors: I. Y. Iourov, S. G. Vorsanova, M. A. Zelenova, K. S. Vasin, O. S. Kurinnaia, S. A. Korostelev, Yu. B. Yurov

Institutions: Pirogov Russian National Research Medical University, Sechenov University

Language: Russian

Topic: Genetic Syndromes and Imprinting

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2961997261

FWCI: 0.638

Cites: 33

Cited by: 10

Related to: 10