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Phenotypic Characterization of Murine Models of Cerebral Cavernous Malformations

Cerebral cavernous malformations (CCMs) are clusters of dilated capillaries that affect around 0.5% of the population. CCMs exist in two forms, sporadic and familial. Mutations in 3 documented genes, KRIT1 (CCM1), CCM2 and PDCD10 (CCM3), cause the autosomal dominant form of the disease, and somatic...

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Publicado en:Lab Invest
Autores principales: Zeineddine, Hussein A., Girard, Romuald, Saadat, Laleh, Shen, Le, Lightle, Rhonda, Moore, Thomas, Cao, Ying, Hobson, Nick, Shenkar, Robert, Avner, Kenneth, Chaudager, Kiranj, Koskimäki, Janne, Polster, Sean P., Fam, Maged D., Shi, Changbin, Lopez-Ramirez, Miguel Alejandro, Tang, Alan T., Gallione, Carol, Kahn, Mark L., Ginsberg, Mark, Marchuk, Douglas A., Awad, Issam A.
Formato: Artigo
Lenguaje:Inglês
Publicado: 2018
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC6309944/
https://ncbi.nlm.nih.gov/pubmed/29946133
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41374-018-0030-y
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