Chinese capillary malformation-arteriovenous malformation: clinical and genetic analysis of eight cases
BackgroundCapillary malformation-arteriovenous malformation (CM-AVM) is an inherited autosomal dominant vascular disorder associated with RAS p21 protein activator (RASA1) or EPH receptor B4 (EPHB4) mutations. We aimed to investigate the clinical features of eight Chinese families with CM-AVM and th...
Guardat en:
| Autors principals: | , , , , , |
|---|---|
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Frontiers Media S.A.
2026-03-01
|
| Col·lecció: | Frontiers in Medicine |
| Matèries: | |
| Accés en línia: | https://www.frontiersin.org/articles/10.3389/fmed.2026.1774495/full |
| Etiquetes: |
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|