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Cerebral Cavernous Malformations: Somatic Mutations in Vascular Endothelial Cells

OBJECTIVE: Germline mutations in three genes have been found in familial cases of cerebral cavernous malformations (CCM). We previously discovered somatic and germline truncating mutations in the KRIT1 gene supporting the “two-hit” mechanism of CCM lesion formation in a single lesion. The purpose of...

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Detaylı Bibliyografya
Asıl Yazarlar: Gault, Judith, Awad, Issam A., Recksiek, Peter, Shenkar, Robert, Breeze, Robert, Handler, Michael, Kleinschmidt-DeMasters, Bette Kay
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2009
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2722441/
https://ncbi.nlm.nih.gov/pubmed/19574835
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1227/01.NEU.0000348049.81121.C1
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