Novel CCM1, CCM2, and CCM3 mutations in patients with cerebral cavernous malformations: in-frame deletion in CCM2 prevents formation of a CCM1/CCM2/CCM3 protein complex-Reference-Cited by-同舟云学术

Novel CCM1, CCM2, and CCM3 mutations in patients with cerebral cavernous malformations: in-frame deletion in CCM2 prevents formation of a CCM1/CCM2/CCM3 protein complex

Published:2008-02-25 Issue:5 Volume:29 Page:709-717
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Stahl Sonja,Gaetzner Sabine,Voss Katrin,Brackertz Bettina,Schleider Elisa,Sürücü Oguzkan,Kunze Ekkehard,Netzer Christian,Korenke Christoph,Finckh Ulrich,Habek Mario,Poljakovic Zdravka,Elbracht Miriam,Rudnik-Schöneborn Sabine,Bertalanffy Helmut,Sure Ulrich,Felbor Ute

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.20712/fullpdf

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4. Genotype-phenotype correlations in cerebral cavernous malformations patients;Denier;Ann Neurol,2006

5. Genetics of cerebral cavernous angioma;Felbor;Zentralbl Neurochir,2006

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