Zou A

No ORCID on file · 1 paper in corpus
2024
Orphanet journal of rare diseases ·doi:10.1186/s13023-024-03404-6

BackgroundFactor XII (FXII or F12) deficiency is a rare inherited disorder, typically lacking haemorrhagic symptoms. There is limited literature exists on FXII deficiency and mutations within the Chinese population. This study aimed to char…