A Case of a Novel Perforin Gene Variant in Severe Familial Hemophagocytic Lymphohistiocytosis Type 2 (FHL2).

Yamauchi H, Hino M, Meguro K, Nakano T, Aoki T, Yamashita Y, Okunushi T, Yamamoto T, Sato H, Yasumi T, Hirata Y, Shibata H, Nakajima H, Hamada H

Open source

DOI
10.1155/crh/1949986
Published
2026
Container
Case reports in hematology
Publisher
Not recorded
Open access
yes

Credibility signals

uncertain Score 53/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.

Show all credibility signals

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