For: | Liu XY, Nie YB, Chen XJ, Gao XH, Zhai LJ, Min FL. Adult onset type 2 familial hemophagocytic lymphohistiocytosis with PRF1 c.65delC/c.163C>T compound heterozygous mutations: A case report. World J Clin Cases 2021; 9(10): 2289-2295 [PMID: 33869605 DOI: 10.12998/wjcc.v9.i10.2289] |
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URL: | https://www.wjgnet.com/2307-8960/full/v9/i10/2289.htm |
Number | Citing Articles |
1 |
Yuan Shi, Zhidong Qiao, Xiaoduo Bi, Chenxin Zhang, Junxian Fu, Yuexin Jia, Guanglu Yang. RF1 Gene Mutation in Familial Hemophagocytic Lymphohistiocytosis 2: A Family Report and Literature Review. Pharmacogenomics and Personalized Medicine 2021; : 1637 doi: 10.2147/PGPM.S326921
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2 |
Marina Sham, Rongbo Zhu, Daniele Merico, Yehonatan Pasternak. Whole exome sequencing identifies causative compound heterozygous variants in PRF1 in late-onset familial hemophagocytic lymphohistiocytosis. LymphoSign Journal 2022; 9(4): 85 doi: 10.14785/lymphosign-2022-0014
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3 |
Xiangke Xin, Na Wang, Yicheng Zhang. Hemophagocytic lymphohistiocytosis with a hemizygous PRF1 c.674G>A mutation. The American Journal of the Medical Sciences 2023; 366(5): 387 doi: 10.1016/j.amjms.2023.07.005
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4 |
A case report of adult type 2 familial hemophagocytic lymphohistiocytosis. Precision Medical Sciences 2023; 12(4): 260 doi: 10.1002/prm2.12120
|