Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly

BACKGROUND: Autism spectrum disorder (ASD), a developmental disorder of early childhood onset, affects males four times more frequently than females, suggesting a role for the sex chromosomes. In this study, we describe a family with ASD in which a predicted pathogenic nonsense mutation in the X-chr...

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Detalles Bibliográficos
Autores principales: Woodbury-Smith, Marc, Deneault, Eric, Yuen, Ryan K. C., Walker, Susan, Zarrei, Mehdi, Pellecchia, Giovanna, Howe, Jennifer L., Hoang, Ny, Uddin, Mohammed, Marshall, Christian R., Chrysler, Christina, Thompson, Ann, Szatmari, Peter, Scherer, Stephen W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5679329/
https://www.ncbi.nlm.nih.gov/pubmed/29152164
http://dx.doi.org/10.1186/s13229-017-0175-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5679329/
https://www.ncbi.nlm.nih.gov/pubmed/29152164
http://dx.doi.org/10.1186/s13229-017-0175-3

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