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Less severe clinical manifestations in patients with hereditary angioedema with missense C1INH gene mutations

✍ Scribed by Bors, Andras; Csuka, Dorottya; Varga, Lilian; Farkas, Henriette; Tordai, Attila; Füst, George; Szilagyi, Agnes

No coin nor oath required. For personal study only.

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