Recurrent deletion of ZNF630 at Xp11.23 is not associated with mental retardation.

doi:10.1002/ajmg.a.33292

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Article

Recurrent deletion of ZNF630 at Xp11.23 is not associated with mental retardation.

American journal of medical genetics. Part A - 1 Mar 2010

Lugtenberg Dorien, Zangrande-Vieira Luiz, Kirchhoff Maria, Whibley Annabel C, Oudakker Astrid R, Kjaergaard Susanne, Vianna-Morgante Angela M, Kleefstra Tjitske, Ruiter Mariken, Jehee Fernanda S, Ullmann Reinhard, Schwartz Charles E, Stratton Michael, Raymond F Lucy, Veltman Joris A, Vrijenhoek Terry, Pfundt Rolph, Schuurs-Hoeijmakers Janneke H M, Hehir-Kwa Jayne Y, Froyen Guy, Chelly Jamel, Ropers Hans Hilger, Moraine Claude, Gècz Jozef, Knijnenburg Jeroen, Kant Sarina G, Hamel Ben C J, Rosenberg Carla, van Bokhoven Hans, de Brouwer Arjan P M

Abstract excerpt

ZNF630 is a member of the primate-specific Xp11 zinc finger gene cluster that consists of six closely related genes, of which ZNF41, ZNF81, and ZNF674 have been shown to be involved in mental retardation. This suggests that mutations of ZNF630 might influence cognitive function. Here, we detected...

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Identifiers

PMID: 20186789
DOI: 10.1002/ajmg.a.33292

Genes

ZNF41
ZNF81

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20186789-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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