Ann Lab Med 2017; 37(2): 162-165  https://doi.org/10.3343/alm.2017.37.2.162
Familial Hemophagocytic Lymphohistiocytosis Type 2 in a Korean Infant With Compound Heterozygous PRF1 Defects Involving a PRF1 Mutation, c.1091T>G
Min-Sun Kim, M.D.1, Young-Uk Cho, M.D.1, Seongsoo Jang, M.D.1, Eul-Ju Seo, M.D.1, Ho Joon Im, M.D.2, and Chan-Jeoung Park, M.D.1
Departments of Laboratory Medicine1 and Pediatrics2, University of Ulsan, College of Medicine and Asan Medical Center, Seoul, Korea
Correspondence to: Young-Uk Cho
Department of Laboratory Medicine, University of Ulsan, College of Medicine and Asan Medical Center, 88 Olympic-ro 43-gil, Songpa-gu, Seoul 05505, Korea
Tel: +82-2-3010-4501, Fax: +82-2-478-0884, E-mail: yucho@amc.seoul.kr
Received: June 2, 2016; Revised: September 29, 2016; Accepted: December 9, 2016; Published online: March 1, 2017.
© The Korean Society for Laboratory Medicine. All rights reserved.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.


This Article

e-submission

Archives

Indexed/Covered by