Insights From Genetic Studies of Cerebral Palsy

Cohort-based whole exome and whole genome sequencing and copy number variant (CNV) studies have identified genetic etiologies for a sizable proportion of patients with cerebral palsy (CP). These findings indicate that genetic mutations collectively comprise an important cause of CP. We review findin...

Descripción completa

Detalles Bibliográficos
Autores principales: Lewis, Sara A., Shetty, Sheetal, Wilson, Bryce A., Huang, Aris J., Jin, Sheng Chih, Smithers-Sheedy, Hayley, Fahey, Michael C., Kruer, Michael C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7859255/
https://www.ncbi.nlm.nih.gov/pubmed/33551980
http://dx.doi.org/10.3389/fneur.2020.625428

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7859255/
https://www.ncbi.nlm.nih.gov/pubmed/33551980
http://dx.doi.org/10.3389/fneur.2020.625428

Ejemplares similares