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Mutations in the guanine nucleotide exchange factor gene IQSEC2 cause nonsyndromic intellectual disability.

Authors :
Shoubridge C
Tarpey PS
Abidi F
Ramsden SL
Rujirabanjerd S
Murphy JA
Boyle J
Shaw M
Gardner A
Proos A
Puusepp H
Raymond FL
Schwartz CE
Stevenson RE
Turner G
Field M
Walikonis RS
Harvey RJ
Hackett A
Futreal PA
Stratton MR
Gécz J
Source :
Nature genetics [Nat Genet] 2010 Jun; Vol. 42 (6), pp. 486-8. Date of Electronic Publication: 2010 May 16.
Publication Year :
2010

Abstract

The first family identified as having a nonsyndromic intellectual disability was mapped in 1988. Here we show that a mutation of IQSEC2, encoding a guanine nucleotide exchange factor for the ADP-ribosylation factor family of small GTPases, caused this disorder. In addition to MRX1, IQSEC2 mutations were identified in three other families with X-linked intellectual disability. This discovery was made possible by systematic and unbiased X chromosome exome resequencing.

Details

Language :
English
ISSN :
1546-1718
Volume :
42
Issue :
6
Database :
MEDLINE
Journal :
Nature genetics
Publication Type :
Academic Journal
Accession number :
20473311
Full Text :
https://doi.org/10.1038/ng.588