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Rare IDH1 variants are common in pediatric hemispheric diffuse astrocytomas and frequently associated with Li-Fraumeni syndrome
D. Sumerauer, L. Krskova, A. Vicha, A. Misove, Y. Mamatjan, P. Jencova, M. Vlckova, L. Slamova, K. Vanova, P. Liby, J. Taborsky, M. Koblizek, R. Klubal, M. Kyncl, G. Zadeh, J. Stary, J. Zamecnik, V. Ramaswamy, M. Zapotocky
Acta neuropathologica.
2020 ;
139 (4) :
795-797.
[pub] 20200103
Language English Country Germany
Document type Journal Article, Research Support, Non-U.S. Gov't
Persistent link
https://www.medvik.cz/link/bmc21020642
Online
Full text
NLK
ProQuest Central
from 1997-01-01 to 1 year ago
Health & Medicine (ProQuest)
from 1997-01-01 to 1 year ago
Psychology Database (ProQuest)
from 1997-01-01 to 1 year ago
- MeSH
- Astrocytoma complications genetics MeSH
- Child MeSH
- Isocitrate Dehydrogenase genetics MeSH
- Humans MeSH
- Li-Fraumeni Syndrome complications genetics MeSH
- Adolescent MeSH
- Mutation MeSH
- Tumor Suppressor Protein p53 genetics MeSH
- Brain Neoplasms complications genetics MeSH
- Check Tag
- Child MeSH
- Humans MeSH
- Adolescent MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Department of Neurosurgery Toronto Western Hospital University of Toronto Toronto ON Canada
Departments of Medical Biophysics and Paediatrics University of Toronto Toronto ON Canada
References provided by Crossref.org
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