Work

MECP2 Mutations in Sporadic Cases of Rett Syndrome Are Almost Exclusively of Paternal Origin

Year: 2001

Type: article

Study design: Observational Study

Source: The American Journal of Human Genetics

DOI: 10.1086/320109

Authors: R. Trappe, F. Laccone, J. Cobilanschi, M. Meins, P. Huppke, F. Hanefeld, W. Engel

Institution: University of Göttingen

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

OpenAlex ID: W2049128446

FWCI: 7.344

Cites: 33

Cited by: 288

Related to: 8