| Literature DB >> 25156961 |
N Okamoto1, F Miya2, T Tsunoda2, M Kato3, S Saitoh4, M Yamasaki5, A Shimizu6, C Torii7, Y Kanemura8,9, K Kosaki7.
Abstract
We developed a next-generation sequencing (NGS) based mutation screening strategy for neurodevelopmental diseases. Using this system, we screened 284 genes in 40 patients. Several novel mutations were discovered. Patient 1 had a novel mutation in ACTB. Her dysmorphic feature was mild for Baraitser-Winter syndrome. Patient 2 had a truncating mutation of DYRK1A. She lacked microcephaly, which was previously assumed to be a constant feature of DYRK1A loss of function. Patient 3 had a novel mutation in GABRD gene. She showed Rett syndrome like features. Patient 4 was diagnosed with Noonan syndrome with PTPN11 mutation. He showed complete agenesis of corpus callosum. We have discussed these novel findings.Entities:
Keywords: Baraitser-Winter syndrome; DYRK1A; GABRD; next-generation sequencing
Mesh:
Substances:
Year: 2014 PMID: 25156961 DOI: 10.1111/cge.12492
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438