Kctd13-deficient mice display short-term memory impairment and sex-dependent genetic interactions

The 16p11.2 BP4-BP5 deletion and duplication syndromes are associated with a complex spectrum of neurodevelopmental phenotypes that includes developmental delay and autism spectrum disorder, with a reciprocal effect on head circumference, brain structure and body mass index. Mouse models of the 16p1...

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Detalles Bibliográficos
Publicado en:Hum Mol Genet
Main Authors: Arbogast, Thomas, Razaz, Parisa, Ellegood, Jacob, McKinstry, Spencer U, Erdin, Serkan, Currall, Benjamin, Aneichyk, Tanya, Lerch, Jason P, Qiu, Lily R, Rodriguiz, Ramona M, Henkelman, R M, Talkowski, Michael E, Wetsel, William C, Golzio, Christelle, Katsanis, Nicholas
Formato: Artigo
Idioma:Inglês
Publicado: Oxford University Press 2019
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General Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6489413/
https://ncbi.nlm.nih.gov/pubmed/30590535
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddy436
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