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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Parkinsons Dis
Päätekijät: Chiang, Han-Lin, Chen, Chiung Mei, Chen, Yi-Chun, Chao, Chih-Ying, Wu, Yih-Ru, Lee-Chen, Guey-Jen
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Hindawi 2020
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7196998/
https://ncbi.nlm.nih.gov/pubmed/32377332
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2020/9582317
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