COQ2 V393A confers high risk susceptibility for multiple system atrophy in East Asian population

Multiple system atrophy (MSA) is a rare, late-onset, and devastating neurodegenerative disease characterized by autonomic failure, alongside with various combination of parkinsonism, cerebellar ataxia, and pyramidal dysfunction. Since we first identified biallelic mutations in the COQ2 gene in two m...

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Veröffentlicht in:	Journal of the neurological sciences 2021-10, Vol.429, p.117623-117623, Article 117623
Hauptverfasser:	Porto, Kristine Joyce, Hirano, Makito, Mitsui, Jun, Chikada, Ayaka, Matsukawa, Takashi, Ishiura, Hiroyuki, Toda, Tatsushi, Kusunoki, Susumu, Tsuji, Shoji
Format:	Artikel
Sprache:	eng
Schlagworte:	Asian continental ancestry group Case-control studies Multiple system atrophy Mutation
Online-Zugang:	Volltext
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