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Article

Differences in behavioural phenotype between parental deletion and maternal uniparental disomy in Prader-Willi syndrome: an ERP study.

Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology - 1 Jun 2005

Stauder Johannes E A, Boer Harm, Gerits Rolf H A, Tummers Anke, Whittington Joyce, Curfs Leopold M G

Abstract excerpt

OBJECTIVE: Paternal deletion and maternal uniparental disomy are the principal genetic subtypes associated with Prader-Willi syndrome (PWS). Recent clinical findings suggest differences in phenotype between these subtypes. The present experimental study addresses this issue using a cognitive psycho-physiological setup. METHODS: Behaviour and event-related brain activity (ERP) was recorded by a continuous...

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Identifiers

PMID: 15978509
DOI: 10.1016/j.clinph.2005.02.019

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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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