A carregar...

CHCHD10 is involved in the development of Parkinson’s disease caused by CHCHD2 loss-of-function mutation p.T61I

Previously we identified the p.Thr61Ile mutation in coiled-coil-helix-coiled-coil-helix domain containing 2 (CHCHD2) in a Chinese family with autosomal dominant Parkinson’s disease. But the mechanism is still unclear. In this study, we explored the effects of CHCHD2 p.Thr61Ile mutation in cells and...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Neurobiol Aging
Main Authors: Mao, Chengyuan, Wang, Herui, Luo, Haiyang, Zhang, Shuyu, Xu, Huisha, Zhang, Shuo, Rosenblum, Jared, Wang, Zhilei, Zhang, Qi, Tang, Mibo, Shepard, Matthew J., Wang, Xiang, Wang, Yaohe, Zhuang, Zhengping, Shi, Changhe, Xu, Yuming
Formato: Artigo
Idioma:Inglês
Publicado em: 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8320701/
https://ncbi.nlm.nih.gov/pubmed/30530185
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neurobiolaging.2018.10.020
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!