ARHGEF9 disease: Phenotype clarification and genotype-phenotype correlation

OBJECTIVE: We aimed to generate a review and description of the phenotypic and genotypic spectra of ARHGEF9 mutations. METHODS: Patients with mutations or chromosomal disruptions affecting ARHGEF9 were identified through our clinics and review of the literature. Detailed medical history and examinat...

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Detalles Bibliográficos
Autores principales: Alber, Michael, Kalscheuer, Vera M., Marco, Elysa, Sherr, Elliott, Lesca, Gaetan, Till, Marianne, Gradek, Gyri, Wiesener, Antje, Korenke, Christoph, Mercier, Sandra, Becker, Felicitas, Yamamoto, Toshiyuki, Scherer, Stephen W., Marshall, Christian R., Walker, Susan, Dutta, Usha R., Dalal, Ashwin B., Suckow, Vanessa, Jamali, Payman, Kahrizi, Kimia, Najmabadi, Hossein, Minassian, Berge A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5446782/
https://www.ncbi.nlm.nih.gov/pubmed/28589176
http://dx.doi.org/10.1212/NXG.0000000000000148

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5446782/
https://www.ncbi.nlm.nih.gov/pubmed/28589176
http://dx.doi.org/10.1212/NXG.0000000000000148

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