De novo POGZ mutations in sporadic autism disrupt the DNA-binding activity of POGZ

BACKGROUND: A spontaneous de novo mutation is a new mutation appeared in a child that neither the parent carries. Recent studies suggest that recurrent de novo loss-of-function mutations identified in patients with sporadic autism spectrum disorder (ASD) play a key role in the etiology of the disord...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:J Mol Psychiatry
Main Authors: Matsumura, Kensuke, Nakazawa, Takanobu, Nagayasu, Kazuki, Gotoda-Nishimura, Nanaka, Kasai, Atsushi, Hayata-Takano, Atsuko, Shintani, Norihito, Yamamori, Hidenaga, Yasuda, Yuka, Hashimoto, Ryota, Hashimoto, Hitoshi
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2016
Assuntos:
Short Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4839133/
https://ncbi.nlm.nih.gov/pubmed/27103995
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40303-016-0016-x
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados