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

Stephanie Ong; Manabu Funayama; Yuki Mangyoku; Hiromichi Kawai; Hiroyo Yoshino; Yuanzhe Li; Kenya Nishioka; Nobutaka Hattori

doi:10.1002/mds.29692

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

Mov Disord. 2024 Mar;39(3):626-627. doi: 10.1002/mds.29692. Epub 2023 Dec 25.

Authors

Stephanie Ong^{1

2}, Manabu Funayama^{1

2

3}, Yuki Mangyoku¹, Hiromichi Kawai⁴, Hiroyo Yoshino³, Yuanzhe Li^{1

5}, Kenya Nishioka^{1

6}, Nobutaka Hattori^{1

2

3

7}

Affiliations

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.

PMID: 38146173
DOI: 10.1002/mds.29692

No abstract available

Publication types

Letter

MeSH terms

Chromosome Deletion
DiGeorge Syndrome* / genetics
Humans
Japan
Parkinsonian Disorders* / genetics

Publication types

MeSH terms

Grants and funding