Ann Lab Med 2019; 39(2): 229-231
The First Case of Congenital Prekallikrein Deficiency in Korea With a Novel Pathogenic Variant (c.1198G>T)
Sohee Ryu, M.D.1, Ja-Yoon Gu, B.S.2, Kyung Taek Hong, M.D.3, Doo Hee Han, M.D., Ph.D.4, and Hyun Kyung Kim, M.D., Ph.D.1,2
1Department of Laboratory Medicine, 2Cancer Research Institute, Departments of 3Pediatrics and 4Otorhinolaryngology, Seoul National University College of Medicine, Seoul, Korea
Corresponding author: Hyun Kyung Kim, M.D.
Department of Laboratory Medicine, Seoul National University College of Medicine, 101 Daehak-ro, Jongno-gu, Seoul 03080, Korea
Tel: +82-2-2072-0853, Fax: +82-2-747-0359, E-mail:
Received: April 19, 2018; Revised: June 11, 2018; Accepted: September 20, 2018; Published online: March 1, 2019.
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