De Novo Mutations in Patients with Ataxic CP
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.
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
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Pediatric Neurology Briefs Publishers
2015-09-01
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| Series: | Pediatric Neurology Briefs |
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| Online Access: | https://www.pediatricneurologybriefs.com/articles/111 |