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

APOE genetic variability in an Egyptian cohort of PD

埃及帕金森病患者队列中APOE基因变异情况

Khedr, Eman M; William, Martina B; Elhosseiny, Aliaa A; Shalash, Ali; Fawi, Gharib; Yousef, Mohamed H; El-Jaafary, Shaimaa; Lee, Hamin; Jama, Alina; Koraym, Mohamed; Helmy, Asmaa; Salah, Yara; George, Peter; Haridy, Nourelhoda A; Nabhan, Samir; Atputhavadivel, Agsha; Elfarrash, Sara; Ragab, Gaafar; Hegazy, Mohamed Tharwat; Elsaid, Yasmin; Gabr, Asmaa S; Shebl, Nourhan; Aly, Lobna; Abdelwahhab, Nesreen; Belal, Tamer M; Elsayed, Nehal A B; El-Gamal, Mohamed; Elgamal, Shimaa; Ragab, Salma; Mekky, Jaidaa; Houlden, Henry; Rizig, Mie; Salama, Mohamed

The p.Gly2019Ser is a common LRRK2 pathogenic variant among Egyptians with familial and sporadic Parkinson's disease

p.Gly2019Ser是埃及家族性和散发性帕金森病患者中常见的LRRK2致病变异。

William, Martina B; Hamed, Sharifa; Shalash, Ali; Khedr, Eman M; Yousef, Mohamed H; El-Jaafary, Shaimaa; Fawi, Gharib; Helmy, Asmaa; Hamid, Eman; Essam, Mohamed; Lee, Hamin; Jama, Alina; Koraym, Mohamed; Mahmoud, Doaa M; Elfarrash, Sara; Elsaid, Yasmin; Gabr, Asmaa S; Shebl, Nourhan; Abdelwahhab, Nesreen; Belal, Tamer M; Elsayed, Nehal A B; El-Gamal, Mohamed; Elgamal, Shimaa; Ragab, Salma; Mekky, Jaidaa; Aly, Lobna; Nabhan, Samir; Ragab, Gaafar; Hussein, Mohamed A; Hegazy, Mohamed Tharwat; Houlden, Henry; Salama, Mohamed; Rizig, Mie