IDH Mutations: Genotype-Phenotype Correlation and Prognostic Impact

IDH1/2 mutation is the most frequent genomic alteration found in gliomas, affecting 40% of these tumors and is one of the earliest alterations occurring in gliomagenesis. We investigated a series of 1305 gliomas and showed that IDH mutation is almost constant in 1p19q codeleted tumors. We found that...

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Detalles Bibliográficos
Autores principales: Wang, Xiao-Wei, Ciccarino, Pietro, Rossetto, Marta, Boisselier, Blandine, Marie, Yannick, Desestret, Virginie, Gleize, Vincent, Mokhtari, Karima, Sanson, Marc, Labussière, Marianne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022066/
https://www.ncbi.nlm.nih.gov/pubmed/24877111
http://dx.doi.org/10.1155/2014/540236

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022066/
https://www.ncbi.nlm.nih.gov/pubmed/24877111
http://dx.doi.org/10.1155/2014/540236

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