Whole‐exome sequencing for variant discovery in blepharospasm-Reference-Cited by-同舟云学术

Whole‐exome sequencing for variant discovery in blepharospasm

Published:2018-05-16 Issue:4 Volume:6 Page:601-626
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Tian Jun¹²,Vemula Satya R.¹^ORCID,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.¹^ORCID

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

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.411

Reference100 articles.

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