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pro vyhledávání: '"Rajkamalpreet S Mann"'
Publikováno v:
Journal of Integrative Neuroscience, Vol 23, Iss 3, p 63 (2024)
Background: Rats with a loss-of-function mutation in the contactin-associated protein-like 2 (Cntnap2) gene have been validated as an animal model of autism spectrum disorder (ASD). Similar to many autistic individuals, Cntnap2 knock-out rats (Cntnap
Externí odkaz:
https://doaj.org/article/0e9ede3f3b734b5c9179b0f4994e3745
Publikováno v:
Anatomy and Cell Biology Publications
The contactin-associated protein-like 2 gene, CNTNAP2, is a highly penetrant risk gene thought to play a role in the genetic etiology of language-related disorders, such as autism spectrum disorder and developmental language disorder. Despite its can
Autor:
Ashley L. Schormans, Susanne Schmid, Kaela E. Scott, Rajkamalpreet S Mann, Karnig Kazazian, Dorit Möhrle, Brian L. Allman
Publikováno v:
Brain and Mind Institute Researchers' Publications
Autism spectrum disorder (ASD) is characterized by social interaction and communication impairments, as well as restrictive/repetitive patterns of behavior, interests or activities, which can coexist with intellectual disability and altered sensory p