Gonadal mosaicism of a novel IQSEC2 variant causing female limited intellectual disability and epilepsy

We report a family with four girls with moderate to severe intellectual disability and epilepsy. Two girls showed regression in adolescence and died of presumed sudden unexpected death in epilepsy at 16 and 22 years. Whole exome sequencing identified a truncating pathogenic variant in IQSEC2 at NM_0...

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Detalhes bibliográficos
Publicado no:Eur J Hum Genet
Main Authors: Ewans, Lisa J, Field, Michael, Zhu, Ying, Turner, Gillian, Leffler, Melanie, Dinger, Marcel E, Cowley, Mark J, Buckley, Michael F, Scheffer, Ingrid E, Jackson, Matilda R, Roscioli, Tony, Shoubridge, Cheryl
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2017
Assuntos:
Short Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5477359/
https://ncbi.nlm.nih.gov/pubmed/28295038
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2017.29
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