A 15q14 microdeletion involving MEIS2 identified in a patient with autism spectrum disorder

We describe a 9-year-old male patient with a 15q14 microdeletion including MEIS2. The patient was born with a ventricular septal defect and submucosal cleft. Mild developmental disability and autism spectrum disorder diagnosed in childhood were also considered to be consequences of MEIS2 haploinsuff...

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Bibliografiske detaljer
Udgivet i:Hum Genome Var
Main Authors: Shimojima, Keiko, Ondo, Yumiko, Okamoto, Nobuhiko, Yamamoto, Toshiyuki
Format: Artigo
Sprog:Inglês
Udgivet: Nature Publishing Group 2017
Fag:
Data Report
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5517666/
https://ncbi.nlm.nih.gov/pubmed/28736618
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/hgv.2017.29
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