reference/12787734

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/12787734

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endingPage	557
issn	1460-2083 0964-6906
issueIdentifier	3
pageRange	546-557
publicationName	Human Molecular Genetics
startingPage	546
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bibliographicCitation	Sollis E, Graham SA, Vino A, Froehlich H, Vreeburg M, Dimitropoulou D, Gilissen C, Pfundt R, Rappold GA, Brunner HG, Deriziotis P, Fisher SE. Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder. Hum Mol Genet. 2016 Feb 01;25(3):546–57. doi: 10.1093/hmg/ddv495. PMID: 26647308.
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date	2015-12-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/26647308 https://doi.org/10.1093/hmg/ddv495
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Identification and functional characterization ofde novo FOXP1variants provides novel insights into the etiology of neurodevelopmental disorder
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