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t/gene-prf1

PRF1 gene

Discuss publications and research concerning the PRF1 gene.

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Related literature

The genetic architecture of multiple sclerosis in 2026: From susceptibility to disease progression.
PRF1
Case Report: Primary hemophagocytic lymphohistiocytosis with a homozygous PRF1 variant: a case suggesting early immunoporosis and an expanded phenotypic spectrum.
PRF1
Familial Hemophagocytic Lymphohistiocytosis Due to PRF1 Mutation Triggered by Enterovirus.
PRF1
Characterization of a novel splicing mutation in UNC13D gene through amplicon sequencing: a case report on HLH.
PRF1
Finding a Balance between Protection and Pathology: The Dual Role of Perforin in Human Disease.
PRF1
Perforin gene mutation in familial haemophagocytic lymphohistiocytosis: the first reported case from Hong Kong.
PRF1
Novel STXBP2 mutation causing familial hemophagocytic lymphohistiocytosis.
PRF1
A665G mutation in PRF1 in a Turkish infant with familial hemophagocytic lymphohistiocytosis.
PRF1
Temperature sensitivity of human perforin mutants unmasks subtotal loss of cytotoxicity, delayed FHL, and a predisposition to cancer.
PRF1
Variations of the perforin gene in patients with multiple sclerosis.
PRF1

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