Targeted resequencing identifies genes with recurrent variation in cerebral palsy

A growing body of evidence points to a considerable and heterogeneous genetic aetiology of cerebral palsy (CP). To identify recurrently variant CP genes, we designed a custom gene panel of 112 candidate genes. We tested 366 clinically unselected singleton cases with CP, including 271 cases not previ...

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Publicado en:NPJ Genom Med
Main Authors: van Eyk, C. L., Corbett, M. A., Frank, M. S. B., Webber, D. L., Newman, M., Berry, J. G., Harper, K., Haines, B. P., McMichael, G., Woenig, J. A., MacLennan, A. H., Gecz, J.
Formato: Artigo
Idioma:Inglês
Publicado: Nature Publishing Group UK 2019
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Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6828700/
https://ncbi.nlm.nih.gov/pubmed/31700678
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41525-019-0101-z
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