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Neurobehavioral phenotype of autism spectrum disorder associated with germline heterozygous mutations in PTEN

Germline mutations in PTEN, the gene that encodes phosphatase and tensin homolog, have been identified in up to 20% of children with autism spectrum disorder (ASD) and macrocephaly and are associated with marked abnormalities in the white matter of the brain. This study sought to characterize the ne...

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Detalhes bibliográficos
Publicado no:Transl Psychiatry
Main Authors: Busch, Robyn M., Srivastava, Siddharth, Hogue, Olivia, Frazier, Thomas W., Klaas, Patricia, Hardan, Antonio, Martinez-Agosto, Julian A., Sahin, Mustafa, Eng, Charis
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2019
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6783427/
https://ncbi.nlm.nih.gov/pubmed/31594918
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41398-019-0588-1
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