Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

A665G mutation in PRF1 in a Turkish infant with familial hemophagocytic lymphohistiocytosis.

Pediatric blood & cancer - 1 Feb 2011

Aslan Deniz

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Base Sequence
Share to PRF1 gene
Share to Infant
Share to Lymphohistiocytosis, Hemophagocytic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Perforin

Share to Pore Forming Cytotoxic Proteins

Share to Turkey

Source

Identifiers

PMID: 21157897
DOI: 10.1002/pbc.22867

Genes

PRF1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A665G mutation in PRF1 in a Turkish infant with familial hemophagocytic lymphohistiocytosis.PMID 21157897Read ↗

PRF1 gene mutation in a Saudi patient with haemophagocytic lymphohistiocytosis.Semantic proximity Read ↗

Familial Hemophagocytic Lymphohistiocytosis Type 2 in a Korean Infant With Compound Heterozygous PRF1 Defects Involving a PRF1 Mutation, c.1091T>G.Semantic proximity Read ↗

Familial Hemophagocytic Lymphohistiocytosis Due to PRF1 Mutation Triggered by Enterovirus.Semantic proximity Read ↗

Hemophagocytic lymphohistiocytosis with a hemizygous PRF1 c.674G>A mutation.Semantic proximity Read ↗

Unusual Prominent Pulmonary Involvement in a Homozygous PRF1 Gene Variant in a Female Patient.Semantic proximity Read ↗

A novel pathogenic variant in PRF1 associated with hemophagocytic lymphohistiocytosis.Semantic proximity Read ↗

A novel PTF1A mutation in a patient with severe pancreatic and cerebellar involvement.Semantic proximity Read ↗

Mutations in the perforin gene in children with hemophagocytic lymphohistiocytosis.Semantic proximity Read ↗

Genetic variant spectrum in 265 Chinese patients with hemophagocytic lymphohistiocytosis: Molecular analyses of PRF1, UNC13D, STX11, STXBP2, SH2D1A, and XIAP.Semantic proximity Read ↗

Familial Hemophagocytic Lymphohistiocytosis Type 2 in a Chinese Infant with PRF1 Homozygous Mutation: a Case Report.Semantic proximity Read ↗

Genetic background of FHLH in Qatar: Registry data and population studySemantic proximity Read ↗

Genetic background of FHLH in Qatar: Registry data and population studySemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.