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Reconsideration of biallelic inactivation of the VHL tumour suppressor gene in hemangioblastomas of the central nervous system

OBJECTIVES—Cerebellar haemangioblastoma occurs sporadically or as a component tumour of autosomal dominant von Hippel-Lindau disease. Biallelic inactivation of the VHL tumour suppressor gene, which is located on chromosome 3p, has been shown to be involved in the pathogenesis of both tumour entities...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Glasker, S, Bender, B, Apel, T, van Velthoven, V, Mulligan, L, Zentner, J, Neumann, H
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BMJ Group 2001
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1737358/
https://ncbi.nlm.nih.gov/pubmed/11309459
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp.70.5.644
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