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

Detalles Bibliográficos
Autores principales:	Kim, Min-Sun, Cho, Young-Uk, Jang, Seongsoo, Seo, Eul-Ju, Im, Ho Joon, Park, Chan-Jeoung
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Korean Society for Laboratory Medicine 2017
Materias:	Letter to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5203996/ https://www.ncbi.nlm.nih.gov/pubmed/28029005 http://dx.doi.org/10.3343/alm.2017.37.2.162

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