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Metabolomics‐based identification of metabolic alterations in PARK2
OBJECTIVE: Parkin is the causative gene for autosomal recessive familial Parkinson's disease (PD), although it remains unclear how parkin dysfunction is involved with the general condition. Recently, serum and/or plasma metabolomics revealed alterations in metabolic pathways that might reflect...
Uloženo v:
| Vydáno v: | Ann Clin Transl Neurol |
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| Hlavní autoři: | , , , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
John Wiley and Sons Inc.
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6414487/ https://ncbi.nlm.nih.gov/pubmed/30911576 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.724 |
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