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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Publicat a:Sci Rep
Autors principals: 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
Idioma:Inglês
Publicat: Nature Publishing Group UK 2019
Matèries:
Article
Accés en línia: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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