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

EUROPEAN JOURNAL OF HUMAN GENETICS(2015)

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摘要
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.
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Genetics research,Biomedicine,general,Human Genetics,Bioinformatics,Gene Expression,Cytogenetics
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