Identification of two de novo variants causing inherited antithrombin deficiency by quantitative analysis of variant alleles

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Published in:Thrombosis research 2024-01, Vol.233, p.37-40
Main Authors: Togashi, Tomoki, Nagaya, Satomi, Meguro-Horike, Makiko, Matsumoto, Haruto, Imai, Yuta, Yamaguchi, Koichi, Fujii, Yoshinari, Moriya, Haruka, Kikuchi, Yuika, Yasuda, Ibuki, Horike, Shin-Ichi, Morishita, Eriko
Format: Article
Language:English
Subjects:
Alleles
Antithrombin III - genetics
Antithrombin III Deficiency - genetics
Antithrombins
Humans
Thrombophilia - genetics
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container_title Thrombosis research
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creator Togashi, Tomoki
Nagaya, Satomi
Meguro-Horike, Makiko
Matsumoto, Haruto
Imai, Yuta
Yamaguchi, Koichi
Fujii, Yoshinari
Moriya, Haruka
Kikuchi, Yuika
Yasuda, Ibuki
Horike, Shin-Ichi
Morishita, Eriko
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doi_str_mv 10.1016/j.thromres.2023.11.016
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subjects Alleles
Antithrombin III - genetics
Antithrombin III Deficiency - genetics
Antithrombins
Humans
Thrombophilia - genetics
title Identification of two de novo variants causing inherited antithrombin deficiency by quantitative analysis of variant alleles
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