Absence of mutations at <em>SERPINI1</em> gene in a cohort of patients with Cerebral Cavernous Malformations
Cerebral cavernous malformations (CCM) are vascular lesions affecting brain microvessels. While molecular bases of the sporadic condition are not yet well elucidated, familial forms arise following mutations at three different loci KRIT1, CCM2 and PDCD10. However, no germline mutations are detected...
| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
PAGEPress Publications
2021-09-01
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| Series: | Journal of Biological Research |
| Subjects: | |
| Online Access: | https://pagepressjournals.org/index.php/jbr/article/view/9838 |