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...

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Detalhes bibliográficos
Publicado no:Front Neurol
Main Authors: Lewis, Sara A., Shetty, Sheetal, Wilson, Bryce A., Huang, Aris J., Jin, Sheng Chih, Smithers-Sheedy, Hayley, Fahey, Michael C., Kruer, Michael C.
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2021
Assuntos:
Neurology
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7859255/
https://ncbi.nlm.nih.gov/pubmed/33551980
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2020.625428
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