A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigrees

BACKGROUND: Although several genetic variants for autism spectrum disorder (ASD) have now been identified, these largely occur sporadically or are de novo. Much less progress has been made in identifying inherited variants, even though the disorder itself is familial in the majority of cases. The ob...

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Detalles Bibliográficos
Autores principales: Woodbury-Smith, Marc, Paterson, Andrew D., O’Connor, Irene, Zarrei, Mehdi, Yuen, Ryan K. C., Howe, Jennifer L, Thompson, Ann, Parlier, Morgan, Fernandez, Bridget, Piven, Joseph, Scherer, Stephen W., Vieland, Veronica, Szatmari, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5996536/
https://www.ncbi.nlm.nih.gov/pubmed/29890955
http://dx.doi.org/10.1186/s11689-018-9238-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5996536/
https://www.ncbi.nlm.nih.gov/pubmed/29890955
http://dx.doi.org/10.1186/s11689-018-9238-9

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