RT Journal Article
SR Electronic
T1 <em>WDR45</em> mutations may cause a <em>MECP2</em> mutation-negative Rett syndrome phenotype
JF Neurology Genetics
JO Neurol Genet
FD Lippincott Williams &amp; 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