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Initial diagnoses given to persons with the fragile X associated tremor/ataxia syndrome (FXTAS)

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Year: 2005
Type: article
Study design: Observational Study
Source: Neurology
DOI: 10.1212/01.wnl.0000168900.86323.9c
Authors: D. A. Hall, E. Berry-Kravis, S. Jacquemont, C. D. Rice, J. Cogswell, L. Zhang, R. J. Hagerman, P. J. Hagerman, M. A. Leehey
Institutions: Rush University Medical Center, University of Colorado Health, University of California Davis Medical Center, University of California, Davis
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 Institute of Neurological Disorders and Stroke, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Awards: G1500619533, Neurological Phenotype in FMR1 Premutation Carriers, G2471754898, Genotype-Phenotype Relationships in Fragile X Families
OpenAlex ID: W2000080960
FWCI: 6.987
Cites: 11
Cited by: 115
Related to: 10
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