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Article

Epigenetic control of the immune system: a lesson from Kabuki syndrome.

Immunologic research - 1 Apr 2016

Stagi Stefano, Gulino Anna Virginia, Lapi Elisabetta, Rigante Donato

Abstract excerpt

Kabuki syndrome (KS) is a rare multi-systemic disorder characterized by a distinct face, postnatal growth deficiency, mild-to-moderate intellectual disability, skeletal and visceral (mainly cardiovascular, renal, and skeletal) malformations, dermatoglyphic abnormalities. Its cause is related to mutations of two genes: KMT2D (histone-lysine N-methyltransferase 2D) and KDM6A (lysine-specific demethylase 6A), both...

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Identifiers

PMID: 26411453
DOI: 10.1007/s12026-015-8707-4

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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