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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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2018
Materias:
Original Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5846809/
https://www.ncbi.nlm.nih.gov/pubmed/28771244
http://dx.doi.org/10.1038/gim.2017.83

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5846809/
https://www.ncbi.nlm.nih.gov/pubmed/28771244
http://dx.doi.org/10.1038/gim.2017.83

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