Work

Histone Modifications Depict an Aberrantly Heterochromatinized FMR1 Gene in Fragile X Syndrome

Year: 2002

Type: article

Source: The American Journal of Human Genetics

DOI: 10.1086/342931

Authors: Bradford Coffee, Fuping Zhang, Stephanie Ceman, Stephen T. Warren, Daniel Reines

Institutions: Emory University, Howard Hughes Medical Institute

Language: English

Topic: Genetics and Neurodevelopmental Disorders

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: bronze

Funders: FRAXA Research Foundation, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Award: A PROGRAM OF INVESTIGATION INTO FRAGILE X SYNDROME

OpenAlex ID: W2121012521

FWCI: 3.721

Cites: 38

Cited by: 202

Related to: 10