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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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Transl Psychiatry
Päätekijät: Busch, Robyn M., Srivastava, Siddharth, Hogue, Olivia, Frazier, Thomas W., Klaas, Patricia, Hardan, Antonio, Martinez-Agosto, Julian A., Sahin, Mustafa, Eng, Charis
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Nature Publishing Group UK 2019
Aiheet:
Linkit: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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