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Partial duplications of the ATRX gene cause the ATR-X syndrome

Authors :
Jean-Pierre Fryns
Catherine Badens
Koen Devriendt
Guy Froyen
Joris Vermeesch
Hilde Van Esch
Caroline Lacoste
Bernard Thienpont
Dominique Van Schoubroeck
Thorny De Ravel
Philippe Moerman
Clinical sciences
Medical Genetics
Source :
European Journal of Human Genetics. 15:1094-1097
Publication Year :
2007
Publisher :
Springer Science and Business Media LLC, 2007.

Abstract

ATR-X syndrome is a rare syndromic X-linked mental retardation disorder. We report that some of the patients suspected of ATR-X carry large intragenic duplications in the ATRX gene, leading to an absence of ATRX mRNA and of the protein. These findings underscore the need for including quantitative analyses to mutation analysis of the ATRX gene.

Details

ISSN :
14765438 and 10184813
Volume :
15
Database :
OpenAIRE
Journal :
European Journal of Human Genetics
Accession number :
edsair.doi.dedup.....55edcf0c1d8b81935e7cdc4a15501b06
Full Text :
https://doi.org/10.1038/sj.ejhg.5201878