De Novo Mutations in Patients with Ataxic CP.
Publication/Presentation Date
8-1-2015
Abstract
As a part of a large study investigating childhood ataxias in the UK and Switzerland, Schnekenberg et al. analyzed the genetic associations with congenital cerebellar ataxia in 10 patients using either a targeted next generation sequencing panel of 118 genes or trio-based exome sequencing.
Volume
29
Issue
8
First Page
62
Last Page
62
ISSN
1043-3155
Published In/Presented At
Agarwal, S., & Emrick, L. (2015). De Novo Mutations in Patients with Ataxic CP. Pediatric neurology briefs, 29(8), 62. https://doi.org/10.15844/pedneurbriefs-29-8-5
Disciplines
Medicine and Health Sciences | Pediatrics
PubMedID
26933599
Department(s)
Department of Pediatrics
Document Type
Article
COinS