reference/10041784

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/10041784

Outgoing Links

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contentType	Journal Article\|Research Support, Non-U.S. Gov't
endingPage	6494
issn	0964-6906 1460-2083
issueIdentifier	24
pageRange	6481-6494
publicationName	Human Molecular Genetics
startingPage	6481
bibliographicCitation	Segura-Puimedon M, Sahún I, Velot E, Dubus P, Borralleras C, Rodrigues AJ, Valero MC, Valverde O, Sousa N, Herault Y, Dierssen M, Pérez-Jurado LA, Campuzano V. Heterozygous deletion of the Williams-Beuren syndrome critical interval in mice recapitulates most features of the human disorder. Hum Mol Genet. 2014 Dec 15;23(24):6481–94. doi: 10.1093/hmg/ddu368. PMID: 25027326.
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date	2014-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/25027326 https://doi.org/10.1093/hmg/ddu368
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Heterozygous deletion of the Williams–Beuren syndrome critical interval in mice recapitulates most features of the human disorder
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