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. 2009 Apr 23;17(5):697. doi: 10.1038/ejhg.2008.262

Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy

Dorien Lugtenberg, Tjitske Kleefstra, Astrid R Oudakker, Willy M Nillesen, Helger G Yntema, Andreas Tzschach, Martine Raynaud, Dietz Rating, Hubert Journel, Jamel Chelly, Cyril Goizet, Didier Lacombe, Jean-Michel Pedespan, Bernard Echenne, Gholamali Tariverdian, Declan O'Rourke, Mary D King, Andrew Green, Margriet van Kogelenberg, Hilde Van Esch, Jozef Gecz, Ben CJ Hamel, Hans van Bokhoven, Arjan PM de Brouwer
PMCID: PMC2986260

Correction to: European Journal of Human Genetics (2009) 17, 444–453; doi:10.1038/ejhg.2008.208; published online 5 November 2008

Since the publication of this paper, the authors have noticed that Declan O'Rourke's and Mary D King's affiliation number 10 should read ‘Childrens University Hospital, Temple Street, Dublin, Ireland'.

The authors would like to apologise for this mistake.

Articles from European Journal of Human Genetics are provided here courtesy of Nature Publishing Group

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