Published 2015 | Version v1.0.0
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De Novo Mutations in Patients with Ataxic CP

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.

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PNB-29-62

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2015
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