Work

Mild overexpression of MeCP2 causes a progressive neurological disorder in mice

Year: 2004

Type: article

Source: Human Molecular Genetics

DOI: 10.1093/hmg/ddh282

Authors: Ann L. Collins, Jonathan M. Levenson, Alexander P. Vilaythong, Ronald Richman, Dawna L. Armstrong, Jeffrey L. Noebels, J. David Sweatt, Huda Y. Zoghbi

Institution: Baylor College of Medicine

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: closed

Funders: National Institutes of Health, National Institute of Mental Health, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: G1890955776, G2415555256, G4236449247, Baylor Intellectual and Developmental Disabilities Research Center, G644223529, Pathophysiology of Rett Syndrome /MECP2 Mutations, Biochemical Mechanisms of Neural Plasticity, Functional Studies in Rett Syndrome

OpenAlex ID: W2155388782

FWCI: 11.25

Cites: 55

Cited by: 626

Related to: 10