Familial Hemophagocytic Lymphohistiocytosis Type 2 in a Korean Infant With Compound Heterozygous PRF1 Defects Involving a PRF1 Mutation, c.1091T>G

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Bibliographic Details
Published in:Annals of laboratory medicine 2017, Vol.37 (2), p.162-165
Main Authors: Kim, Min Sun, Cho, Young Uk, Jang, Seongsoo, Seo, Eul Ju, Im, Ho Joon, Park, Chan Jeoung
Format: Report
Language:English
Online Access:Get full text
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ISSN:2234-3814
DOI:10.3343/alm.2017.37.2.162