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

Detalles Bibliográficos
Autores principales: Kulikovskaja, Leonora, Sarajlija, Adrijan, Savic-Pavicevic, Dusanka, Dobricic, Valerija, Klein, Christine, Westenberger, Ana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2018
Materias:
Clinical/Scientific Notes
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5873728/
https://www.ncbi.nlm.nih.gov/pubmed/29600274
http://dx.doi.org/10.1212/NXG.0000000000000227

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5873728/
https://www.ncbi.nlm.nih.gov/pubmed/29600274
http://dx.doi.org/10.1212/NXG.0000000000000227

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