Whole‐exome sequencing for variant discovery in blepharospasm

Author:

Tian Jun12,Vemula Satya R.1ORCID,Xiao Jianfeng1,Valente Enza Maria34,Defazio Giovanni56,Petrucci Simona7,Gigante Angelo Fabio5,Rudzińska‐Bar Monika8,Wszolek Zbigniew K.9,Kennelly Kathleen D.9,Uitti Ryan J.9,van Gerpen Jay A.9,Hedera Peter10,Trimble Elizabeth J.1,LeDoux Mark S.1ORCID

Affiliation:

1. Departments of Neurology and Anatomy and Neurobiology University of Tennessee Health Science Center Memphis Tennessee

2. Department of Neurology Second Affiliated Hospital School of Medicine Zhejiang University Hangzhou Zhejiang China

3. Department of Molecular Medicine University of Pavia Pavia Italy

4. Neurogenetics Unit IRCCS Santa Lucia Foundation Rome Italy

5. Department of Basic Clinical Sciences, Neuroscience and Sense Organs Aldo Moro University of Bari Bari Italy

6. Department of Medical Sciences and Public Health University of Cagliari Cagliari Italy

7. Department of Neurology and Psychiatry Sapienza University of Rome Rome Italy

8. Department of Neurology Faculty of Medicine Medical University of Silesia Katowice Poland

9. Department of Neurology Mayo Clinic Florida Jacksonville Florida

10. Department of Neurology Vanderbilt University Nashville Tennessee

Funder

National Institute of Neurological Disorders and Stroke

National Institute on Aging

U.S. Department of Defense

Benign Essential Blepharospasm Research Foundation

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

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