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

Internet

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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