Delphine Charignon
0000-0003-3423-0608
5 papers found
Refreshing results…
Plasminogen glycoforms alteration and activation susceptibility associated with the missense variant p.Lys330Glu in HAE‐PLG patients
SERPING1 mutation update: Mutation spectrum and C1 Inhibitor phenotypes
Angioedema
SERPING1 and F12 combined variants in a hereditary angioedema family
Hereditary C1 inhibitor deficiency is associated with high spontaneous amidase activity
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