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Lab Reports | 
Tracy Hampton, PhD
JAMA. 2013;310(1):22. doi:10.1001/jama.2013.7876.

JAMA Clinical Challenge | 
Brian J. Dlouhy, MD; Jeremy D. W. Greenlee, MD
JAMA. 2012;307(20):2195-2196. doi:10.1001/jama.2012.3447.

Original Contribution |  FREE
Sébastien Jacquemont, MD; Randi J. Hagerman, MD; Maureen A. Leehey, MD; et al.
JAMA. 2004;291(4):460-469. doi:10.1001/jama.291.4.460.

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From The JAMA Network
JAMA Neurology
Original Investigation  | 
Expanding the Clinical Phenotype Associated With ELOVL4 Mutation:  Study of a Large French-Canadian Family With Autosomal Dominant Spinocerebellar Ataxia and Erythrokeratodermia
Maxime Cadieux-Dion, BSc; Maude Turcotte-Gauthier, MSc; Anne Noreau, MSc; et al.
JAMA Neurology
Case Report/Case Series  | 
Aggressive Course in Encephalitis With Opsoclonus, Ataxia, Chorea, and Seizures:  The First Pediatric Case of γ-Aminobutyric Acid Type B Receptor Autoimmunity
Michael C. Kruer, MD; Romana Hoeftberger, MD; Kit Yeng Lim, MD; et al.
JAMA Neurology
Clinical Pathologic Conference  | 
A Rare Adult Cause of Dizziness
Francy Shu, MD; Robert Oberle, MD; Emily Herndon, MD; et al.
JAMA Neurology
Original Investigation  | 
SYNE1 Mutations in Autosomal Recessive Cerebellar Ataxia
Anne Noreau, MSc; Cynthia V. Bourassa, MSc; Anna Szuto, MSc; et al.