De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy

PURPOSE: Hemiplegia is a subtype of cerebral palsy (CP) in which one side of the body is affected. Our earlier study of unselected children with CP demonstrated de novo and clinically relevant rare inherited genomic copy-number variations (CNVs) in 9.6% of participants. Here, we examined the prevale...

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Detaylı Bibliyografya
Yayımlandı:Genet Med
Asıl Yazarlar: Zarrei, Mehdi, Fehlings, Darcy L, Mawjee, Karizma, Switzer, Lauren, Thiruvahindrapuram, Bhooma, Walker, Susan, Merico, Daniele, Casallo, Guillermo, Uddin, Mohammed, MacDonald, Jeffrey R, Gazzellone, Matthew J, Higginbotham, Edward J, Campbell, Craig, deVeber, Gabrielle, Frid, Pam, Gorter, Jan Willem, Hunt, Carolyn, Kawamura, Anne, Kim, Marie, McCormick, Anna, Mesterman, Ronit, Samdup, Dawa, Marshall, Christian R, Stavropoulos, Dimitri J, Wintle, Richard F, Scherer, Stephen W
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Nature Publishing Group 2018
Konular:
Original Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5846809/
https://ncbi.nlm.nih.gov/pubmed/28771244
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/gim.2017.83
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