Associated Papers
Clinically observed RASA1 missense mutants exhibit diverse RasGAP protein behaviors.
Paul ME et al.
Biorxiv : the Preprint Server for Biology, 2025
41256670 (PubMed )
Supplement: media-1.pdf
EphrinB2-EphB4-RASA1 Signaling in Human Cerebrovascular Development and Disease.
Zeng X et al.
Trends in Molecular Medicine, 2019
RASA1 mutations and associated phenotypes in 68 families with capillary malformation-arteriovenous malformation.
Revencu N et al.
Human Mutation, 2013
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