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...

Description complète

Enregistré dans:
Détails bibliographiques
Publié dans:Sci Rep
Auteurs principaux: 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
Langue:Inglês
Publié: Nature Publishing Group UK 2019
Sujets:
Article
Accès en ligne: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
Tags: Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!

Documents similaires