Mutation Analysis of CCM1, CCM2 and CCM3 Genes in a Cohort of Italian Patients with Cerebral Cavernous Malformation-Reference-Cited by-同舟云学术

Mutation Analysis of CCM1, CCM2 and CCM3 Genes in a Cohort of Italian Patients with Cerebral Cavernous Malformation

Published:2010-10-04 Issue:2 Volume:21 Page:215-224
ISSN:1015-6305
Container-title:Brain Pathology
language:en
Short-container-title:

Author:

D'Angelo Rosalia,Marini Valeria,Rinaldi Carmela,Origone Paola,Dorcaratto Alessandra,Avolio Maria,Goitre Luca,Forni Marco,Capra Valeria,Alafaci Concetta,Mareni Cristina,Garrè Cecilia,Bramanti Placido,Sidoti Antonina,Retta Saverio Francesco,Amato Aldo

Publisher

Wiley

Subject

Neurology (clinical),Pathology and Forensic Medicine,General Neuroscience

Reference46 articles.

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3. Mutations within the programmed cell death 10 gene cause cerebral cavernous malformations;Bergametti;Am J Hum Genet,2005

4. Listening to silence and understanding nonsense: exonic mutations that affect splicing;Cartegni;Nat Rev Genet,2002

5. C329X in KRIT1 is a founder mutation among CCM patients in Sardinia;Cau;Eur J Med Genet,2009

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