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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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| Pubblicato in: | Hum Genome Var |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Nature Publishing Group
2017
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| Soggetti: | |
| Accesso online: | 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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