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A rare sequence variant in intron 1 of THAP1 is associated with primary dystonia.

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第一作者: Satya R,Vemula
第一单位: Departments of Neurology and Anatomy & Neurobiology, University of Tennessee Health Science Center Memphis, Tennessee, 38163.
作者单位: Departments of Neurology and Anatomy & Neurobiology, University of Tennessee Health Science Center Memphis, Tennessee, 38163. [1] Bastian Voice Institute Downers Grove, Illinois. [2] Department of Neurology, Washington University School of Medicine St. Louis, Missouri. [3] Department of Otolaryngology-Head and Neck Surgery, Washington University School of Medicine St. Louis, Missouri. [4] Department of Neurology, Mayo Clinic Jacksonville, Florida, 32224. [5] Department of Neurology, Vanderbilt University Nashville, Tennessee. [6] Parkinson's & Movement Disorder Institute Fountain Valley, California, 92708. [7] New York Center for Voice and Swallowing Disorders New York, New York. [8] Department of Neurology, Jagiellonian University Medical College in Krakow Kraków, Poland. [9] Clinic for Child Neurology and Psychiatry, Medical Faculty University of Belgrade Belgrade, Serbia. [10] Departments of Neurology, Human Genetics, and Pediatrics, School of Medicine, Emory University Atlanta, Georgia, 30322. [11] Department of Neurology, Loma Linda University Health System Loma Linda, California, 92354. [12]
DOI 10.1002/mgg3.67
PMID 24936516
发布时间 2021-10-21
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Molecular genetics & genomic medicine

Molecular genetics & genomic medicine

2014年2卷3期

261-72页

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