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Neuropathy as a presenting feature in fragile X‐associated tremor/ataxia syndrome

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Year: 2007
Type: article
Study design: Case Report
Source: American Journal of Medical Genetics Part A
DOI: 10.1002/ajmg.a.31920
Authors: Randi J. Hagerman, Sarah M. Coffey, Ricardo Maselli, Kultida Soontarapornchai, James A. Brunberg, Maureen A. Leehey, Lin Zhang, Louise W. Gane, Grace Fenton‐Farrell, Flora Tassone, Paul J. 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: MIND Institute, University of California, Davis, 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: G1064348956, G1855666826, G3041847283, G3306906556, Action tremor & dementia in male carriers of fragile X, Research in Intellectual and Developmental Disabilities, Fragile X-associated Tremor/Ataxia Syndrome, Genotype-Phenotype Relationships in Fragile X Families
OpenAlex ID: W2045987259
FWCI: 2.536
Cites: 23
Cited by: 64
Related to: 10
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