reference/13636446

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/13636446

Outgoing Links

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contentType	Journal Article\|Research Support, Non-U.S. Gov't
endingPage	1796
issn	1098-3600
issueIdentifier	8
pageRange	1790-1796
publicationName	Genetics in medicine : official journal of the American College of Medical Genetics
startingPage	1790
bibliographicCitation	Iqbal Z, Tawamie H, Ba W, Reis A, Halak BA, Sticht H, Uebe S, Kasri NN, Riazuddin S, van Bokhoven H, Abou Jamra R. Loss of function of SVBP leads to autosomal recessive intellectual disability, microcephaly, ataxia, and hypotonia. Genet Med. 2019 Aug;21(8):1790–6. doi: 10.1038/s41436-018-0415-8. PMID: 30607023.
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date	201908
identifier	https://doi.org/10.1038/s41436-018-0415-8 https://pubmed.ncbi.nlm.nih.gov/30607023
isPartOf	http://rdf.ncbi.nlm.nih.gov/pubchem/journal/22061 https://portal.issn.org/resource/ISSN/1098-3600
language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Loss of function of SVBP leads to autosomal recessive intellectual disability, microcephaly, ataxia, and hypotonia
discusses	http://id.nlm.nih.gov/mesh/M0552802 http://id.nlm.nih.gov/mesh/M0441466 http://id.nlm.nih.gov/mesh/M0028143 http://id.nlm.nih.gov/mesh/M0576996 http://id.nlm.nih.gov/mesh/M0003559 http://id.nlm.nih.gov/mesh/M0475820
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Total number of triples: 47.