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

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

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

Afiliação

Ong S; Department of Neurology, Faculty of Medicine, Juntendo University, Tokyo, Japan.
Funayama M; International Collaborative Research Administration, Juntendo University, Tokyo, Japan.
Mangyoku Y; Department of Neurology, Faculty of Medicine, Juntendo University, Tokyo, Japan.
Kawai H; International Collaborative Research Administration, Juntendo University, Tokyo, Japan.
Yoshino H; Research Institute for Diseases of Old Age, Graduate School of Medicine, Juntendo University, Tokyo, Japan.
Li Y; Department of Neurology, Faculty of Medicine, Juntendo University, Tokyo, Japan.
Nishioka K; Department of Neurology, Shiga University of Medical Science, Shiga, Japan.
Hattori N; Research Institute for Diseases of Old Age, Graduate School of Medicine, Juntendo University, Tokyo, Japan.

Mov Disord ; 39(3): 626-627, 2024 Mar.

Article em En | MEDLINE | ID: mdl-38146173

Assuntos

Síndrome de DiGeorge; Transtornos Parkinsonianos; Humanos; Japão; Síndrome de DiGeorge/genética; Transtornos Parkinsonianos/genética; Deleção Cromossômica

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos Parkinsonianos / Síndrome de DiGeorge Limite: Humans País/Região como assunto: Asia Idioma: En Ano de publicação: 2024 Tipo de documento: Article

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