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Article

In Pursuit of New Imprinting Syndromes by Epimutation Screening in Idiopathic Neurodevelopmental Disorder Patients.

BioMed research international - 1 Jan 2015

Mayo Sonia, Monfort Sandra, Roselló Mónica, Oltra Silvestre, Orellana Carmen, Martínez Francisco

Abstract excerpt

Alterations of epigenetic mechanisms, and more specifically imprinting modifications, could be responsible of neurodevelopmental disorders such as intellectual disability (ID) or autism together with other associated clinical features in many cases. Currently only eight imprinting syndromes are defined in spite of the fact that more than 200 genes are known or predicted to be imprinted. Recent publications point...

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Source

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Identifiers

PMID: 26106604
DOI: 10.1155/2015/341986
PMCID: PMC4461700

Genes

SNRPN

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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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