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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Vydáno v:Brain Pathol
Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: Blackwell Publishing Ltd 2010
Témata:
Research Articles
On-line přístup: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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