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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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
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container_issue 2
container_start_page 162
container_title Annals of laboratory medicine
container_volume 37
creator Kim, Min Sun
Cho, Young Uk
Jang, Seongsoo
Seo, Eul Ju
Im, Ho Joon
Park, Chan Jeoung
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doi_str_mv 10.3343/alm.2017.37.2.162
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title 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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