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HAE.12298
HAE.12298
http://dx.doi.org/10.1111/HAE.12298
Severe congenital factor XIII deficiency caused by novel W187X and G273V mutations in the F13A gene; diagnosis and classification according to the ISTH/SSC guidelines.
P356
Q45858519-EE8C8E6D-C17C-491D-8B7F-EF2A68469163
P356
HAE.12298
http://dx.doi.org/10.1111/HAE.12298