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Article

Prader-Willi syndrome: advances in genetics, pathophysiology and treatment.

Trends in endocrinology and metabolism: TEM - 1 Jan 2000

Goldstone Anthony P

Abstract excerpt

Prader-Willi syndrome (PWS) is a complex human genetic disease that arises from lack of expression of paternally inherited imprinted genes on chromosome 15q11-q13. Identification of the imprinting control centre, novel imprinted genes and distinct phenotypes in PWS patients and mouse models has increased interest in this human obesity syndrome. In this review I focus on: (i) the chromosomal region and candidate...

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Identifiers

PMID: 14693421
DOI: 10.1016/j.tem.2003.11.003

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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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