
Genetic variations, including de novo and mitochondrial DNA mutations, play a significant role in the development of cerebral palsy, according to a large-scale whole-genome sequencing study.


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Using whole-genome sequencing, Canadian researchers found a high prevalence of genetic abnormalities in children with cerebral palsy.

Genetic Variants May Contribute to Cerebral Palsy

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Genetic Factors Significantly Contribute to Cerebral Palsy Risk, Whole-Genome Sequencing Study Reveals
