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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Familial Hemophagocytic Lymphohistiocytosis Type 2 in a Korean Infant With Compound Heterozygous PRF1 Defects Involving a PRF1 Mutation, c.1091T>G.
description
2017 nî lūn-bûn
@nan
2017年の論文
@ja
2017年論文
@yue
2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
@wuu
2017年论文
@zh
2017年论文
@zh-cn
name
Familial Hemophagocytic Lympho ...... ng a PRF1 Mutation, c.1091T>G.
@en
Familial Hemophagocytic Lympho ...... ng a PRF1 Mutation, c.1091T>G.
@nl
type
label
Familial Hemophagocytic Lympho ...... ng a PRF1 Mutation, c.1091T>G.
@en
Familial Hemophagocytic Lympho ...... ng a PRF1 Mutation, c.1091T>G.
@nl
prefLabel
Familial Hemophagocytic Lympho ...... ng a PRF1 Mutation, c.1091T>G.
@en
Familial Hemophagocytic Lympho ...... ng a PRF1 Mutation, c.1091T>G.
@nl
P2093
P2860
P1476
Familial Hemophagocytic Lympho ...... ng a PRF1 Mutation, c.1091T>G.
@en
P2093
Chan Jeoung Park
Eul Ju Seo
Ho Joon Im
Min Sun Kim
Seongsoo Jang
Young Uk Cho
P2860
P304
P356
10.3343/ALM.2017.37.2.162
P577
2017-03-01T00:00:00Z