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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Hum Genome Var
Egile Nagusiak: Shimojima, Keiko, Ondo, Yumiko, Okamoto, Nobuhiko, Yamamoto, Toshiyuki
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Nature Publishing Group 2017
Gaiak:
Data Report
Sarrera elektronikoa: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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