Mutations in the von Hippel-Lindau Tumour Suppressor Gene in Central Nervous System Hemangioblastomas

<p>Abstract</p> <p>Central nervous system hemangioblastomas (cHAB) are rare tumours which most commonly arise in the cerebellum. Most tumours are sporadic, but as many as one third of cHABs occur in the course of the hereditary disorder - von Hippel-Lindau disease (VHL). In order to diagnose new VHL...

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Detalhes bibliográficos

Principais autores:	Cybulski Cezary, Matyjasik Joanna, Soroka Marianna, Szymaś Janusz, Górski Bohdan, Dębniak Tadeusz, Jakubowska Anna, Bernaczyk Andrzej, Zimnoch Lech, Bierzyńska-Macyszyn Grażyna, Trojanowski Tomasz, Wierzba-Bobrowicz Teresa, Prudlak Edmund, Markowska-Wojciechowska Alicja, Nowacki Przemysław, Roszkiewicz Andrzej, Kordek Radzisław, Szylberg Tadeusz, Matyja Ewa, Zieliński Krzysztof, Woźniewicz Bogdan, Taraszewska Anna, Kozłowski Wojciech, Lubiński Jan
Formato:	Artigo
Idioma:	Inglês
Publicado em:	BMC 2004-03-01
coleção:	Hereditary Cancer in Clinical Practice
Assuntos:	VHL disease hemangioblastoma germline mutations VHL gene
Acesso em linha:	http://www.hccpjournal.com/content/2/2/93
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