De Novo Mutations in Patients with Ataxic CP.
نویسندگان
چکیده
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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ورودعنوان ژورنال:
- Pediatric neurology briefs
دوره 29 8 شماره
صفحات -
تاریخ انتشار 2015