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

Disciplines

Medicine and Health Sciences | Pediatrics

PubMedID

26933599

Department(s)

Department of Pediatrics

Document Type

Article

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