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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
Jazyk angličtina Země Německo
Typ dokumentu časopisecké články, práce podpořená grantem
Perzistentní odkaz
https://www.medvik.cz/link/bmc21020642
Online
Plný text
NLK
ProQuest Central
od 1997-01-01 do Před 1 rokem
Health & Medicine (ProQuest)
od 1997-01-01 do Před 1 rokem
Psychology Database (ProQuest)
od 1997-01-01 do Před 1 rokem
- MeSH
- astrocytom komplikace genetika MeSH
- dítě MeSH
- isocitrátdehydrogenasa genetika MeSH
- lidé MeSH
- Liův-Fraumeniho syndrom komplikace genetika MeSH
- mladiství MeSH
- mutace MeSH
- nádorový supresorový protein p53 genetika MeSH
- nádory mozku komplikace genetika MeSH
- Check Tag
- dítě MeSH
- lidé MeSH
- mladiství MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem 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
Citace poskytuje Crossref.org
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