Article
Tectonic gene mutations in patients with Joubert syndrome.
European journal of human genetics : EJHG - 1 May 2015
Huppke Peter, Wegener Eike, Böhrer-Rabel Helena, Bolz Hanno J, Zoll Barbara, Gärtner Jutta, Bergmann Carsten
Abstract excerpt
So far very few patients with sequence variants in the closely related tectonic genes TCTN1-3 have been described. By multi-gene panel next-generation sequencing (NGS) in patients with Joubert syndrome, we identified two more patients and summarize what is currently known about the phenotypes associated with sequence variants in these genes. In a boy aged 12 years with intellectual disability and the classical...
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