The First Case of Congenital Prekallikrein Deficiency in Korea With a Novel Pathogenic Variant (c.1198G>T).
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ABSTRACT:
SUBMITTER: Ryu S
PROVIDER: S-EPMC6240513 | biostudies-literature | 2019 Mar
REPOSITORIES: biostudies-literature
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The First Case of Congenital Prekallikrein Deficiency in Korea With a Novel Pathogenic Variant (c.1198G>T).
Ryu Sohee S Gu Ja Yoon JY Hong Kyung Taek KT Han Doo Hee DH Kim Hyun Kyung HK
Annals of laboratory medicine 20190301 2
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