Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson’s Disease

Genetic studies of the familial forms of Parkinson’s disease (PD) have identified a number of causative genes with an established role in its pathogenesis. These genes only explain a fraction of the diagnosed cases. The emergence of Next Generation Sequencing (NGS) expanded the scope of rare variant...

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Bibliografski detalji
Izdano u:Sci Rep
Glavni autori: Yemni, Eman Al, Monies, Dorota, Alkhairallah, Thamer, Bohlega, Saeed, Abouelhoda, Mohamed, Magrashi, Amna, Mustafa, Abeer, AlAbdulaziz, Basma, Alhamed, Mohamed, Baz, Batoul, Goljan, Ewa, Albar, Renad, Jabaan, Amjad, Faquih, Tariq, Subhani, Shazia, Ali, Wafa, Shinwari, Jameela, Al-Mubarak, Bashayer, Al-Tassan, Nada
Format: Artigo
Jezik:Inglês
Izdano: Nature Publishing Group UK 2019
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Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6399448/
https://ncbi.nlm.nih.gov/pubmed/30833663
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-019-40102-x
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