Screening for the FMR1 premutation in Greek patients with late-onset movement disorders
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Geriatrics and Gerontology,Neurology
Reference32 articles.
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1. The FGF14GAA repeat expansion in Greek patients with late‐onset cerebellar ataxia and an overview of the SCA27B phenotype across populations;Clinical Genetics;2024-01-14
2. FMR1 Carriers Report Executive Function Changes Prior to Fragile X‐Associated Tremor/Ataxia Syndrome: A Longitudinal Study;Movement Disorders;2023-12-20
3. A Longitudinal Study of Executive Function in Daily Life in Male Fragile X Premutation Carriers and Association with FXTAS Conversion;2023-09-02
4. Evaluation of the role of FMR1 CGG repeat allele in Parkinson’s disease from the Chinese population;Frontiers in Aging Neuroscience;2023-07-31
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