Identification of a large homozygous VPS13C deletion in a patient with early-onset Parkinsonism-Reference-Cited by-同舟云学术

Identification of a large homozygous VPS13C deletion in a patient with early-onset Parkinsonism

Author:

Darvish Hossein¹,Bravo Paloma²,Tafakhori Abbas³,Azcona Luis J.²⁴,Ranji-Burachaloo Sakineh³,Johari Amir Hossein¹,Paisán-Ruiz Coro²⁵⁶⁷⁸

Affiliation:

1. Department of Medical Genetics; Semnan University of Medical Sciences; Semnan Iran

2. Department of Neurology; Icahn School of Medicine at Mount Sinai, One Gustave L; New York New York USA

3. Iranian Center of Neurological Research, Neuroscience institute; Tehran University of Medical Sciences; Tehran Iran

4. Department of Neurosciences; Icahn School of Medicine at Mount Sinai; New York New York USA

5. Department of Psychiatry; Icahn School of Medicine at Mount Sinai; New York New York USA

6. Department of Genetics and Genomic Sciences; Icahn School of Medicine at Mount Sinai; New York New York USA

7. The Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai; New York New York USA

8. The Friedman Brain and Mindich Child Health and Development Institutes, Icahn School of Medicine at Mount Sinai; New York New York USA

Funder

Shahid Beheshti University of Medical Sciences

American Parkinson Disease Association

National Institute of Neurological Disorders and Stroke

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

Reference5 articles.

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