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Acta Neurologica Belgica
Published in: Acta Neurologica Belgica 5/2020

01-10-2020 | Glioma | Letter to the Editor

Comments on and assessment of “The rs498872 polymorphism is associated with an elevated susceptibility to glioma: a meta-analysis of 36,264 subjects”

Authors: Morteza Gholami, Mahsa M. Amoli, Farshad Sharifi

Published in: Acta Neurologica Belgica | Issue 5/2020

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Excerpt

Dear Editor, …
Literature
1.
Chen B, Li Y, Chen L, Du Y (2019) The rs498872 polymorphism is associated with an elevated susceptibility to glioma: a meta-analysis of 36,264 subjects. Acta Neurol Belg 119(2):239–243CrossRef
2.
Jenkinsa RB, Wrensch MR, Johnson D et al (2011) Distinct germ line polymorphisms underlie gliomamorphologic heterogeneity. Cancer Genet 204(1):13–18CrossRef
3.
Melin B, Dahlin AM, Andersson U et al (2013) Known glioma risk loci are associated with glioma with a family history of brain tumours—a case–control gene association study. Int J Cancer 132:2464–2468CrossRef
4.
Rice T, Zheng S, Decker PA et al (2013) Inherited variant on chromosome 11q23 increases susceptibility to IDH-mutated but not IDH-normal gliomas regardless of grade or histology. Neuro Oncol 15:535–541CrossRef
5.
Yang B, Heng L, Du S et al (2015) Association between RTEL1, PHLDB1, and TREH polymorphisms and glioblastoma risk: a case-control study. Med Sci Monit 21:1983–1988CrossRef
Metadata
Title
Comments on and assessment of “The rs498872 polymorphism is associated with an elevated susceptibility to glioma: a meta-analysis of 36,264 subjects”
Authors
Morteza Gholami
Mahsa M. Amoli
Farshad Sharifi
Publication date
01-10-2020
Publisher
Springer International Publishing
Published in
Acta Neurologica Belgica / Issue 5/2020
Print ISSN: 0300-9009
Electronic ISSN: 2240-2993
DOI
https://doi.org/10.1007/s13760-019-01169-5

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