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publicationName European journal of human genetics : EJHG
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bibliographicCitation Barington M, Risom L, Ek J, Uldall P, Ostergaard E. A recurrent de novo CUX2 missense variant associated with intellectual disability, seizures, and autism spectrum disorder. European Journal of Human Genetics. 2018 May 24;26(9):1–4. doi: 10.1038/s41431-018-0184-5.
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date 2018-05-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://pubmed.ncbi.nlm.nih.gov/29795476
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title A recurrent de novo CUX2 missense variant associated with intellectual disability, seizures, and autism spectrum disorder
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Total number of triples: 36.