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Whole-Exome Sequencing in Searching for New Variants Associated With the Development of Parkinson’s Disease
Background: Parkinson’s disease (PD) is a complex disease with its monogenic forms accounting for less than 10% of all cases. Whole-exome sequencing (WES) technology has been used successfully to find mutations in large families. However, because of the late onset of the disease, only small families...
Tallennettuna:
| Julkaisussa: | Front Aging Neurosci |
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| Päätekijät: | , , , , , , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Frontiers Media S.A.
2018
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5963122/ https://ncbi.nlm.nih.gov/pubmed/29867446 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnagi.2018.00136 |
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