Erratum: Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy (European Journal of Human Genetics (2009) vol. 17 (444-453) 10.1038/ejhg.2008.208)

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 EschJozef Gecz, Ben C.J. Hamel, Hans van Bokhoven, Arjan P.M. de Brouwer

    Research output: Contribution to journalComment/debatepeer-review

    1 Citation (Scopus)
    Original languageEnglish
    Pages (from-to)697
    Number of pages1
    JournalEuropean Journal of Human Genetics
    Volume17
    Issue number5
    DOIs
    Publication statusPublished or Issued - 2009

    ASJC Scopus subject areas

    • Genetics
    • Genetics(clinical)

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