Work

An atypical 12q24.31 microdeletion implicates six genes including a histone demethylase KDM2B and a histone methyltransferase SETD1B in syndromic intellectual disability

Year: 2016

Type: article

Source: Human Genetics

DOI: 10.1007/s00439-016-1668-4

Authors: Jonathan D. J. Labonne, Kang-Han Lee, Shigeki Iwase, Il-Keun Kong, Michael P. Diamond, Lawrence C. Layman, Cheol-Hee Kim, Hyung-Goo Kim

Institutions: Augusta University, Chungnam National University, University of Michigan, Gyeongsang National University

Language: English

Topic: Genomic variations and chromosomal abnormalities

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: Cooley's Anemia Foundation, National Institutes of Health, National Institute of Neurological Disorders and Stroke

Awards: Neutralizing epigenomes in neurodevelopmental disorders, A Neuron-specific Methyl-histone Regulatory Complex

OpenAlex ID: W2340675305

FWCI: 2.993

Cites: 72

Cited by: 60

Related to: 10