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ARHGEF9 mutations cause a specific recognizable X-linked intellectual disability syndrome

Detalles Bibliográficos
Autores principales:	Striano, Pasquale, Zara, Federico
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer 2017
Materias:	Editorial
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5446781/ https://www.ncbi.nlm.nih.gov/pubmed/28589177 http://dx.doi.org/10.1212/NXG.0000000000000159

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