RT Journal Article SR Electronic T1 WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype JF Neurology Genetics JO Neurol Genet FD Lippincott Williams & Wilkins SP e227 DO 10.1212/NXG.0000000000000227 VO 4 IS 2 A1 Kulikovskaja, Leonora A1 Sarajlija, Adrijan A1 Savic-Pavicevic, Dusanka A1 Dobricic, Valerija A1 Klein, Christine A1 Westenberger, Ana YR 2018 UL http://ng.neurology.org/content/4/2/e227.abstract AB