PRICKLE1 Interaction with SYNAPSIN I Reveals a Role in Autism Spectrum Disorders

The frequent comorbidity of Autism Spectrum Disorders (ASDs) with epilepsy suggests a shared underlying genetic susceptibility; several genes, when mutated, can contribute to both disorders. Recently, PRICKLE1 missense mutations were found to segregate with ASD. However, the mechanism by which mutat...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Paemka, Lily, Mahajan, Vinit B., Skeie, Jessica M., Sowers, Levi P., Ehaideb, Salleh N., Gonzalez-Alegre, Pedro, Sasaoka, Toshikuni, Tao, Hirotaka, Miyagi, Asuka, Ueno, Naoto, Takao, Keizo, Miyakawa, Tsuyoshi, Wu, Shu, Darbro, Benjamin W., Ferguson, Polly J., Pieper, Andrew A., Britt, Jeremiah K., Wemmie, John A., Rudd, Danielle S., Wassink, Thomas, El-Shanti, Hatem, Mefford, Heather C., Carvill, Gemma L., Manak, J. Robert, Bassuk, Alexander G.
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2013
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3849077/
https://ncbi.nlm.nih.gov/pubmed/24312498
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0080737
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados