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Article

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

Annals of laboratory medicine - 1 Mar 2017

Kim Min Sun, Cho Young Uk, Jang Seongsoo, Seo Eul Ju, Im Ho Joon, Park Chan Jeoung

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 28029005
DOI: 10.3343/alm.2017.37.2.162
PMCID: PMC5203996

Genes

PRF1

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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