Familial CCM Genes Might Not Be Main Drivers for Pathogenesis of Sporadic CCMs-Genetic Similarity between Cancers and Vascular Malformations.
第一作者:
Jun,Zhang
第一单位:
Departments of Molecular & Translational Medicine (MTM), Texas Tech University Health Science Center El Paso (TTUHSCEP), El Paso, TX 79905, USA.
作者:
关键词
CCM signaling complex (CSC)Cerebral cavernous malformations (CCMs)PIK3CA-related overgrowth spectrum (PROS)developmental venous anomalies (DVAs)familial CCM (fCCM)gain-of-function (GOF)phosphatidylinositol-4, 5-bisphosphate 3-kinase catalytic subunit p110α (PIK3CA)sporadic CCM (sCCM)tumor driver mutationstumor passenger mutationsvascular malformations (VMs)venous malformations (VeMs)
DOI
10.3390/jpm13040673
PMID
37109059
发布时间
2023-05-01
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Journal of personalized medicine
2023年13卷4期
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