Developmental venous anomalies are a genetic primer for cerebral cavernous malformations

Cerebral cavernous malformations (CCM) are a neurovascular anomaly that may occur sporadically, or be inherited due to autosomal dominant mutations in KRIT1, CCM2, or PDCD10. Individual lesions are caused by somatic mutations which have been identified in KRIT1, CCM2, PDCD10, MAP3K3, and PIK3CA. How...

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Detalles Bibliográficos
Autores principales: Snellings, Daniel A., Girard, Romuald, Lightle, Rhonda, Srinath, Abhinav, Romanos, Sharbel, Li, Ying, Chen, Chang, Ren, Aileen A., Kahn, Mark L., Awad, Issam A., Marchuk, Douglas A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8958845/
https://www.ncbi.nlm.nih.gov/pubmed/35355835
http://dx.doi.org/10.1038/s44161-022-00035-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8958845/
https://www.ncbi.nlm.nih.gov/pubmed/35355835
http://dx.doi.org/10.1038/s44161-022-00035-7

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