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Article

Prader-Willi syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain.

Gene expression patterns : GEP - 1 Oct 2003

Lee Syann, Walker Christine L, Wevrick Rachel

Abstract excerpt

Prader-Willi syndrome (PWS) is a neurobehavioral disorder that is due to the loss of multiple, paternally-expressed, imprinted genes on human chromosome 15q11-q13. The candidate genes are conserved in mice and are located in an orthologous region on mouse 7C. Several mouse models in which one or more of the PWS candidate genes are silenced do not recapitulate the full PWS phenotype. We examined the expression...

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Identifiers

PMID: 12971993
DOI: 10.1016/s1567-133x(03)00113-3

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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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