Work

Altered neurodevelopment associated with mutations of RSK2: a morphometric MRI study of Coffin–Lowry syndrome

Year: 2007

Type: article

Study design: Observational Study

Source: Neurogenetics

DOI: 10.1007/s10048-007-0080-6

Authors: Shelli R. Kesler, Richard J. Simensen, Kytja Voeller, Fatima Abidi, Roger E. Stevenson, Charles E. Schwartz, Allan L. Reiss

Institutions: Stanford Medicine, Stanford University, Greenwood Genetic Center

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: green

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

Awards: G1151667499, X-Linked Mental Retardation-Linkage

OpenAlex ID: W2092949245

FWCI: 1.429

Cites: 33

Cited by: 33

Related to: 10