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European Journal of Human Genetics logoLink to European Journal of Human Genetics
. 2015 Apr 16;23(5):720. doi: 10.1038/ejhg.2014.278

Missense variant in CCDC22 causes X-linked recessive intellectual disability with features of Ritscher-Schinzel/3C syndrome

Mateusz Kolanczyk, Peter Krawitz, Jochen Hecht, Anna Hupalowska, Marta Miaczynska, Katrin Marschner, Claire Schlack, Denise Emmerich, Karolina Kobus, Uwe Kornak, Peter N Robinson, Barbara Plecko, Gernot Grangl, Sabine Uhrig, Stefan Mundlos, Denise Horn
PMCID: PMC4402643  PMID: 25880334

Correction to: European Journal of Human Genetics, advance online publication 11 June 2014; doi:10.1038/ejhg.2014.109

The name of one of the authors of this paper was submitted incorrectly. An amendment has been made and the corrected paper appears in this issue.


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

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