VHL mutation analysis in patients with isolated central nervous system haemangioblastoma
Author:
Publisher
Oxford University Press (OUP)
Subject
Clinical Neurology
Link
http://academic.oup.com/brain/article-pdf/130/3/836/782165/awl362.pdf
Reference37 articles.
1. Disruption of oxygen homeostasis underlies congenital Chuvash polycythemia
2. Hemangioblastomas of Central Nervous System: Molecular Genetic Analysis and Clinical Management
3. Contrasting effects on HIF-1alpha regulation by disease-causing pVHL mutations correlate with patterns of tumourigenesis in von Hippel-Lindau disease
4. Germline mutations in the von Hippel-Lindau disease (VHL) gene in Japanese VHL
5. Hypoxia Inducible Factor-α Binding and Ubiquitylation by the von Hippel-Lindau Tumor Suppressor Protein
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