日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Heterozygous PRKN mutations are common but do not increase the risk of Parkinson's disease.

PRKN 杂合突变很常见,但不会增加患帕金森病的风险

Zhu William, Huang Xiaoping, Yoon Esther, Bandres-Ciga Sara, Blauwendraat Cornelis, Billingsley Kimberly J, Cade Joshua H, Wu Beverly P, Williams Victoria H, Schindler Alice B, Brooks Janet, Gibbs J Raphael, Hernandez Dena G, Ehrlich Debra, Singleton Andrew B, Narendra Derek P

CHCHD2 accumulates in distressed mitochondria and facilitates oligomerization of CHCHD10

CHCHD2 在受损线粒体中积累,并促进 CHCHD10 的寡聚化。

Huang, Xiaoping; Wu, Beverly P; Nguyen, Diana; Liu, Yi-Ting; Marani, Melika; Hench, Jürgen; Bénit, Paule; Kozjak-Pavlovic, Vera; Rustin, Pierre; Frank, Stephan; Narendra, Derek P