DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Kulikovskaja L, Sarajlija A, Savic-Pavicevic D, Dobricic V, Klein C, Westenberger A.
WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype.
Neurol Genet 2018;
4 (02) e227
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