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Article

Neurodevelopmental disorders involving genomic imprinting at human chromosome 15q11-q13.

Neurobiology of disease - 1 Jul 2010

Chamberlain Stormy J, Lalande Marc

Abstract excerpt

Human chromosome 15q11-q13 is subject to regulation by genomic imprinting, an epigenetic process by which genes are expressed in a parent-of-origin specific manner. Three neurodevelopmental disorders, Prader-Willi syndrome, Angelman syndrome, and 15q duplication syndrome, result from aberrant expression of imprinted genes in this region. Here, we review the current literature pertaining to mouse models and...

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Identifiers

PMID: 20304067
DOI: 10.1016/j.nbd.2010.03.011

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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