- 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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Kim MS, Cho YU, Jang S, Seo EJ, Im HJ, Park CJ
- KMID: 2373636
- Ann Lab Med.
- 2017 Mar;37(2):162-165.
- doi: 10.3343/alm.2017.37.2.162
No abstract available. -
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