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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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Bibliografiske detaljer
Udgivet i: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
Format: Artigo
Sprog:Inglês
Udgivet: Blackwell Publishing Ltd 2010
Fag:
Online adgang: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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