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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Brain Pathol
Prif Awduron: 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
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Blackwell Publishing Ltd 2010
Pynciau:
Research Articles
Mynediad Ar-lein: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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