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 hypoxia-ind...
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| Principais autores: | , , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Wiley
2020-01-01
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| Serier: | Parkinson's Disease |
| Online adgang: | http://dx.doi.org/10.1155/2020/9582317 |
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