Human Genome Epidemiology Literature Finder
|
Records 1 - 4 (of 4 Records) |
| Query Trace: Disease and L3MBTL3[original query] |
|---|
| Association of SHMT1, MAZ, ERG, and L3MBTL3 Gene Polymorphisms with Susceptibility to Multiple Sclerosis. Biochemical genetics 2019 Jun 57 (3): 355-370. Nazari Mehrabani Seyede Zahra, Shushizadeh Mohammad Hossein, Abazari Mohammad Foad, Nouri Aleagha Maryam, Ardalan Abbas, Abdollahzadeh Rasoul, Azarnezhad Asa |
| Effect of L3MBTL3/PTPN9 polymorphisms on risk to alcohol-induced ONFH in Chinese Han population. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2021 Aug . Xiong Jun, Niu Yi, Liu Wei, Zeng Fan, Cheng Jian-Fei, Chen Shi-Qiang, Zeng Xiang-Zh |
| Identification of the genetic mechanism that associates L3MBTL3 to multiple sclerosis. Human molecular genetics 2022 1 31 (13): 2155-2163. Alcina Antonio, Fedetz Maria, Vidal-Cobo Isabel, Andrés-León Eduardo, García-Sánchez Maria-Isabel, Barroso-Del-Jesus Alicia, Eichau Sara, Gil-Varea Elia, Luisa-Maria Villar , Saiz Albert, Leyva Laura, Vandenbroeck Koen, Otaegui David, Izquierdo Guillermo, Comabella Manuel, Urcelay Elena, Matesanz Fuencis |
| Association of the L3MBTL3 rs1125970 and rs4897367 gene polymorphisms with coronary heart disease susceptibility in the Chinese population: a case-control study. Journal of cardiovascular pharmacology 2023 7 . Yongdong Li, Jiaqiang Zhang, Jun He, Xiaoyu Chen, Xianbo Zhang, Haiqing Wu, Yipeng Di |
- Page last reviewed:Feb 1, 2024
- Content source: