Genetic analysis of IMPDH2 gene in Taiwanese patients with isolated or combined dystonia

The inosine monophosphate dehydrogenase gene (IMPDH2) was recently reported as a novel gene associated with autosomal dominantly inherited dystonia. We investigated 245 Taiwanese patients with molecularly unassigned isolated or combined dystonia without features of neurodevelopmental disorders and f...

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Veröffentlicht in:	Parkinsonism & related disorders 2023-02, Vol.107, p.105294-105294, Article 105294
Hauptverfasser:	Chen, Pin-Shiuan, Wu, Meng-Chen, Tai, Chun-Hwei, Chang, Yung-Yee, Lan, Min-Yu, Chen, Ying-Fa, Lin, Han-I, Lee, Ni-Chung, Lin, Chin-Hsien
Format:	Artikel
Sprache:	eng
Schlagworte:	Asian People - genetics Dystonia Dystonia - genetics Humans IMP Dehydrogenase - genetics IMPDH2 Inosine monophosphate dehydrogenase gene
Online-Zugang:	Volltext
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