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Genetic Analysis of EGLN1 C127S Variant in Taiwanese Parkinson's Disease

Parkinson's disease (PD) is a neurodegenerative disorder related to nigrostriatal dopaminergic neuron degeneration and iron accumulation. As a cellular oxygen sensor, prolyl hydroxylase domain containing protein 2 (PHD2, encoded by egl-9 family hypoxia inducible factor 1, EGLN1) modifies hypoxi...

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Detalles Bibliográficos
Autores principales:	Chiang, Han-Lin, Chen, Chiung Mei, Chen, Yi-Chun, Chao, Chih-Ying, Wu, Yih-Ru, Lee-Chen, Guey-Jen
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi 2020
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7196998/ https://www.ncbi.nlm.nih.gov/pubmed/32377332 http://dx.doi.org/10.1155/2020/9582317

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