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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6828700/
https://www.ncbi.nlm.nih.gov/pubmed/31700678
http://dx.doi.org/10.1038/s41525-019-0101-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6828700/
https://www.ncbi.nlm.nih.gov/pubmed/31700678
http://dx.doi.org/10.1038/s41525-019-0101-z

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