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Molecular and imaging correlates of the fragile X–associated tremor/ataxia syndrome

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Year: 2006
Type: article
Study design: Observational Study
Source: Neurology
DOI: 10.1212/01.wnl.0000239837.57475.3a
Authors: S. Cohen, K. Masyn, J. Adams, D. Hessl, S. Rivera, F. Tassone, J. Brunberg, C. DeCarli, L. Zhang, J. Cogswell, D. Loesch, M. Leehey, J. Grigsby, P. J. Hagerman, R. Hagerman
Institutions: University of California Davis Medical Center, University of California, Davis
Language: English

Topic: Genetic Neurodegenerative Diseases
Subfield: Cellular and Molecular Neuroscience
Field: Neuroscience
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed

Funders: National Institutes of Health, National Institute on Aging, National Institute of Neurological Disorders and Stroke, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Awards: G1264619266, UC Davis Alzheimer's Disease Core Center, G1500619533, G1855666826, Neurological Phenotype in FMR1 Premutation Carriers, G2471754898, G3306906556, Action tremor & dementia in male carriers of fragile X, Research in Intellectual and Developmental Disabilities, Genotype-Phenotype Relationships in Fragile X Families
OpenAlex ID: W1978900628
FWCI: 4.51
Cites: 31
Cited by: 151
Related to: 10
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