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Article

Understanding the biological underpinnings of fragile X syndrome.

Current opinion in pediatrics - 1 Dec 2003

Chiurazzi Pietro, Neri Giovanni, Oostra Ben A

Abstract excerpt

PURPOSE OF REVIEW: The purpose of this review is to present the latest findings on fragile X syndrome and to put them into perspective. Fragile X syndrome is a relatively common form of inherited mental retardation, caused by loss of function of the FMR1 gene on the long arm of the X chromosome. The molecular mechanisms underlying the syndrome are complex and continue to surprise researchers more than 12 years...

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Identifiers

PMID: 14631199
DOI: 10.1097/00008480-200312000-00003

Genes

FMR1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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