Investigation of 22q11.2 Deletion in Japanese Early‐Onset Parkinsonism-Reference-Cited by-同舟云学术

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Investigation of 22q11.2 Deletion in Japanese Early‐Onset Parkinsonism

Published:2023-12-25 Issue: Volume: Page:
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Movement Disorders

Author:

Ong Stephanie¹²^ORCID,Funayama Manabu¹²³^ORCID,Mangyoku Yuki¹,Kawai Hiromichi⁴,Yoshino Hiroyo³,Li Yuanzhe¹⁵,Nishioka Kenya¹⁶,Hattori Nobutaka¹²³⁷

Affiliation:

1. Department of Neurology, Faculty of Medicine Juntendo University Tokyo Japan

2. International Collaborative Research Administration Juntendo University Tokyo Japan

3. Research Institute for Diseases of Old Age, Graduate School of Medicine Juntendo University Tokyo Japan

4. Department of Neurology Shiga University of Medical Science Shiga Japan

5. Department of Diagnosis, Prevention and Treatment of Dementia, Graduate School of Medicine Juntendo University Tokyo Japan

6. Department of Neurology Juntendo Tokyo Koto Geriatric Medical Center Tokyo Japan

7. Neurodegenerative Disorders Collaborative Laboratory, RIKEN Center for Brain Science Saitama Japan

Funder

Japan Society for the Promotion of Science

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference6 articles.

1. Association Between Early-Onset Parkinson Disease and 22q11.2 Deletion Syndrome

2. Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data

3. Large 3-Mb deletions at 22q11.2 locus in Parkinson's disease and schizophrenia

4. Chip-Based Digital PCR Approach Provides A Sensitive and Cost-Effective Single-Day Screening Tool for Common Fetal Aneuploidies—A Proof of Concept Study

5. Screening Newborn Blood Spots for 22q11.2 Deletion Syndrome Using Multiplex Droplet Digital PCR

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