WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype

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Bibliographic Details
Published inNeurology. Genetics Vol. 4; no. 2; p. e227
Main Authors Kulikovskaja, Leonora, Sarajlija, Adrijan, Savic-Pavicevic, Dusanka, Dobricic, Valerija, Klein, Christine, Westenberger, Ana
Format Journal Article
LanguageEnglish
Published United States Wolters Kluwer 01.04.2018
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The Article Processing Charge was funded by Land Schleswig-Holstein within the funding programme Open Access Publikationsfonds.
Funding information and disclosures are provided at the end of the article. Full disclosure form information provided by the authors is available with the full text of this article at Neurology.org/NG.
ISSN:2376-7839
2376-7839
DOI:10.1212/NXG.0000000000000227