Article

Molecular and Cellular Characterization of Primary Endothelial Cells from a Familial Cavernomatosis Patient

2024-02-28

Abstract excerpt

Cerebral cavernous malformations (CCM) or familial cavernomatosis is a rare, autosomal dominant, inherited disease characterized by the presence of vascular malformations consisting of blood vessels with an abnormal structure in the form of clusters. Based on the altered gene (CCM1/Krit1, CCM2, CCM3) and its origin (spontaneous or familial), different types of this dis-ease can be found. In this work we have isola...

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Literature Corpus work: 525c03a5-3c0a-5d39-914f-9f6f0aae2c8b
DOI: 10.20944/preprints202402.1603.v1

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