Involvement of casein kinase 1 epsilon/delta (Csnk1e/d) in the pathogenesis of familial Parkinson's disease caused by CHCHD2

Abstract Parkinson's disease (PD) is a common neurodegenerative disorder that results from the loss of dopaminergic neurons. Mutations in coiled‐coil‐helix‐coiled‐coil‐helix domain containing 2 (CHCHD2) gene cause a familial form of PD with α‐Synuclein aggregation, and we here identified the pathoge...

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Detalhes bibliográficos

Principais autores:	Satoru Torii, Satoko Arakawa, Shigeto Sato, Kei‐ichi Ishikawa, Daisuke Taniguchi, Hajime Tajima Sakurai, Shinya Honda, Yuuichi Hiraoka, Masaya Ono, Wado Akamatsu, Nobutaka Hattori, Shigeomi Shimizu
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Springer Nature 2023-08-01
coleção:	EMBO Molecular Medicine
Assuntos:	CHCHD2 Csnk1e/d α‐Synuclein
Acesso em linha:	https://doi.org/10.15252/emmm.202317451
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