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Article

Molecular evolution of the human SRPX2 gene that causes brain disorders of the Rolandic and Sylvian speech areas.

BMC genetics - 18 Oct 2007

Royer Barbara, Soares Dinesh C, Barlow Paul N, Bontrop Ronald E, Roll Patrice, Robaglia-Schlupp Andrée, Blancher Antoine, Levasseur Anthony, Cau Pierre, Pontarotti Pierre, Szepetowski Pierre

Abstract excerpt

BACKGROUND: The X-linked SRPX2 gene encodes a Sushi Repeat-containing Protein of unknown function and is mutated in two disorders of the Rolandic/Sylvian speech areas. Since it is linked to defects in the functioning and the development of brain areas for speech production, SRPX2 may thus have pa...

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Identifiers

PMID: 17942002
DOI: 10.1186/1471-2156-8-72
PMCID: PMC2151080

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17942002-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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