Type 2 familial hemophagocytic lymphohistiocytosis in half brothers

Author:

Liu Chunxia,Li Ming,Wu Xiaomei,Yao Xiaojian,Zhao Li

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference16 articles.

1. Structural and functional analysis of perforin mutations in association with clinical data of familial hemophagocytic lymphohistiocytosis type 2 (FHL2) patients;An;Protein Sci,2013

2. Expression of porforin and granzyme B in familial hemophagocytic lymphohistiocytosis [in Chinese];Zhou;Zhonghua Xue Ye Xue Za Zhi,2016

3. Hemophagocytic lymphohistiocytosis: updates and evolving concepts;Risma;Current opinion in pediatrics,2012

4. Aberrant maturation of mutant perforin underlies the clinical diversity of hemophagocytic lymphohistiocytosis;Risma;J Clin Invest,2006

5. Association between gene polymorphisms of perforin 1 and hemophagocytic lymphohistiocytosis [in Chinese];Huang;Zhongguo Dang Dai Er Ke Za Zhi,2015

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