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Paper Details

Exploring pathway interactions to detect molecular mechanisms of disease: 22q11.2 deletion syndrome.
Orphanet J Rare Dis
0
2023
22q11, 22q11DS, Akt, CRK like proto-oncogene adaptor protein, PI3K, autistic spectrum disorder, chromosome 22, congenital heart defects, genes, genetic disorder, immune deficiency, natural killer cell, neuropsychiatric diseases, patients, q11, regulated genes, schizophrenia
Author NameAffiliation
Chris T EveloMaastricht University
Chris T EveloMaastricht University
Chris T EveloMaastricht University
Chris T EveloMaastricht University
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Dataset
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Source Link
WikiPathwaysWikiPathways (wikipathways.org) captures the collective knowledge representLink
WikiPathwaysWikiPathways (wikipathways.org) captures the collective knowledge representLink
WikiPathwaysWikiPathways (wikipathways.org) captures the collective knowledge representLink
WikiPathwaysWikiPathways (wikipathways.org) captures the collective knowledge representLink
WikiPathwaysWikiPathways (wikipathways.org) captures the collective knowledge representLink
WikiPathwaysWikiPathways (wikipathways.org) captures the collective knowledge representLink
WikiPathwaysWikiPathways (wikipathways.org) captures the collective knowledge representLink
WikiPathwaysWikiPathways (wikipathways.org) captures the collective knowledge representLink
WikiPathwaysWikiPathways (wikipathways.org) captures the collective knowledge representLink
WikiPathwaysWikiPathways (wikipathways.org) captures the collective knowledge representLink
WikiPathwaysWikiPathways (wikipathways.org) captures the collective knowledge representLink
WikiPathwaysWikiPathways (wikipathways.org) captures the collective knowledge representLink
WikiPathwaysWikiPathways (wikipathways.org) captures the collective knowledge representLink
WikiPathwaysWikiPathways (wikipathways.org) captures the collective knowledge representLink
WikiPathwaysWikiPathways (wikipathways.org) captures the collective knowledge representLink
Release 1.2