LAUSR

Mendelian etiologies identified with whole exome sequencing in cerebral palsy

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1 Published in 2022 at "Annals of Clinical and Translational Neurology"

DOI: 10.1002/acn3.51506

Abstract: Cerebral palsy (CP) is the most common childhood motor disability, yet its link to single‐gene disorders is under‐characterized. To explore the genetic landscape of CP, we conducted whole exome sequencing (WES) in a cohort of… read more here.

Keywords: whole exome; cerebral palsy; mendelian etiologies; exome sequencing ... See more keywords