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

Cerebral cavernous malformations (CCMs) are vascular lesions of the CNS characterized by abnormally enlarged capillary cavities. CCMs can occur as sporadic or familial autosomal dominant form. Familial cases are associated with mutations in CCM1[K‐Rev interaction trapped 1 (KRIT1)], CCM2 (MGC4607) a...

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Detalhes bibliográficos
Publicado no:Brain Pathol
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: Blackwell Publishing Ltd 2010
Assuntos:
Research Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8094256/
https://ncbi.nlm.nih.gov/pubmed/21029238
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1750-3639.2010.00441.x
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