A Case of a Novel Perforin Gene Variant in Severe Familial Hemophagocytic Lymphohistiocytosis Type 2 (FHL2).
- DOI
- 10.1155/crh/1949986
- Published
- 2026
- Container
- Case reports in hematology
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1155/crh/1949986,
title = {A Case of a Novel Perforin Gene Variant in Severe Familial Hemophagocytic Lymphohistiocytosis Type 2 (FHL2).},
author = {Yamauchi H and Hino M and Meguro K and Nakano T and Aoki T and Yamashita Y and Okunushi T and Yamamoto T and Sato H and Yasumi T and Hirata Y and Shibata H and Nakajima H and Hamada H},
year = {2026},
journal = {Case reports in hematology},
doi = {10.1155/crh/1949986},
url = {https://doi.org/10.1155/crh/1949986}
}RIS
TY - JOUR TI - A Case of a Novel Perforin Gene Variant in Severe Familial Hemophagocytic Lymphohistiocytosis Type 2 (FHL2). AU - Yamauchi H AU - Hino M AU - Meguro K AU - Nakano T AU - Aoki T AU - Yamashita Y AU - Okunushi T AU - Yamamoto T AU - Sato H AU - Yasumi T AU - Hirata Y AU - Shibata H AU - Nakajima H AU - Hamada H PY - 2026 JO - Case reports in hematology DO - 10.1155/crh/1949986 UR - https://doi.org/10.1155/crh/1949986 ER -
APA
H, Y., M, H., K, M., T, N., T, A., Y, Y., T, O., T, Y., H, S., T, Y., Y, H., H, S., H, N., & H, H. (2026). A Case of a Novel Perforin Gene Variant in Severe Familial Hemophagocytic Lymphohistiocytosis Type 2 (FHL2).. Case reports in hematology. https://doi.org/10.1155/crh/1949986
Source records
- pubmed · retrieved 2026-09-26T01:54:23.244Z
- europe-pmc · retrieved 2026-09-26T01:54:23.259Z
- doaj · retrieved 2026-09-26T01:54:23.278Z