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Fragile X Premutation Tremor/Ataxia Syndrome: Molecular, Clinical, and Neuroimaging Correlates

The American Journal of Human Genetics · 2003 · Vol. 72(4) · pp. 869–878

Sébastien Jacquemont(University of California Davis Medical Center)Randi J. Hagerman(University of California Davis Medical Center)Maureen A. Leehey(University of Colorado Health)Jim Grigsby(University of Colorado Health)Lin Zhang(University of California Davis Medical Center)James A. Brunberg(University of California Davis Medical Center)Claudia Greco(University of California Davis Medical Center)Vincent des Portes(University of California Davis Medical Center)Tristan Jardini(University of California Davis Medical Center)Richard A. Levine(San Diego State University)Elizabeth Berry‐Kravis(Rush University Medical Center)W. Ted Brown(New York State Office for People With Developmental Disabilities)S. Schaeffer(University of California Davis Medical Center)John T. Kissel(The Ohio State University Wexner Medical Center)Flora Tassone(University of California, Davis)Paul J. Hagerman✉(University of California, Davis)

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Genetics and Neurodevelopmental Disorders Endoplasmic Reticulum Stress and Disease RNA regulation and diseaseParkinsonismAtaxiaIntention tremorCerebellar ataxiaWhite matterMedicinePsychologyMovement disordersWeaknessNeuroscience

MeSH terms

AgedAtaxiaBrainBrain MappingCerebellumEducational StatusEthnicityFragile X SyndromeGenetic Carrier ScreeningHumansMagnetic Resonance ImagingMaleMiddle AgedMutationNerve Tissue Proteins

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Trinucleotide Repeat Disorders