Association of SHMT1, MAZ, ERG, and L3MBTL3 Gene Polymorphisms with Susceptibility to Multiple Sclerosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,General Medicine,Ecology, Evolution, Behavior and Systematics,Biochemistry
Link
http://link.springer.com/content/pdf/10.1007/s10528-018-9894-1.pdf
Reference64 articles.
1. Abdollah Zadeh R, Jalilian N, Sahraian MA, Kasraian Z, Noori-Daloii MR (2017) Polymorphisms of RPS6K B1 and CD86 associates with susceptibility to multiple sclerosis in Iranian population. Neurol Res 39:217–222
2. Abdollahzadeh R, Fard MS, Rahmani F, Moloudi K, Azarnezhad A (2016) Predisposing role of vitamin D receptor (VDR) polymorphisms in the development of multiple sclerosis: a case-control study. J Neurol Sci 367:148–151
3. Abdollahzadeh R, Moradi Pordanjani P, Rahmani F, Mashayekhi F, Azarnezhad A, Mansoori Y (2018) Association of VDR gene polymorphisms with risk of relapsing-remitting multiple sclerosis in an Iranian Kurdish population. Int J Neurosci 128:505–511
4. Anderson DD, Stover PJ (2009) SHMT1 and SHMT2 are functionally redundant in nuclear de novo thymidylate biosynthesis. PLoS ONE 4:e5839
5. Andlauer TF et al (2016) Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation. Sci Adv 2:e1501678
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