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From The JAMA Network
JAMA Neurology
Original Contribution  | 
Fragile X–Associated Tremor/Ataxia Syndrome:  Influence of the FMR1 Gene on Motor Fiber Tracts in Males With Normal and Premutation Alleles
Jun Yi Wang, PhD; David Hessl, PhD; Andrea Schneider, PhD; et al.
JAMA Neurology
Original Contribution  | 
Hereditary Ataxia and Spastic Paraplegia in Portugal:  A Population-Based Prevalence Study
Paula Coutinho, MD, PhD; Luis Ruano, MD, MPH; José L. Loureiro, MD, PhD; et al.
JAMA Neurology
Original Contribution  | 
New Subtype of Spinocerebellar Ataxia With Altered Vertical Eye Movements Mapping to Chromosome 1p32
Carmen Serrano-Munuera, MD; Marc Corral-Juan, BSc; Giovanni Stevanin, PhD; et al.
JAMA Neurology
Observation  | 
Clinical Application of Whole-Exome Sequencing:  A Novel Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay Sequence Variation in a Child With Ataxia
Wendy K. M. Liew, MBChB, MRCPCH; Tawfeg Ben-Omran, MD, FRCPC, FCCMG; Basil T. Darras, MD; et al.