Article

P03-005 - MEFV heterozygous mutations in PFAPA patients

2013-01-01

Abstract excerpt

No abstract is available from the source.

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: fdedf7d5-51a2-5053-83ba-32dddef6c906
DOI: 10.1186/1546-0096-11-s1-a200
PMCID: PMC3952117

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

P03-005 - MEFV heterozygous mutations in PFAPA patientsDOI 10.1186/1546-0096-11-s1-a200Read

PW03-009 – Genetics of PFAPA syndromeSemantic proximity Read

MEFV and NLRP3 gene variants in children with pfapa syndrome in sloveniaSemantic proximity Read

PW01-019 – MEFV gene mutations in 53 periodic fever patientsSemantic proximity Read

The clinical spectrum of 94 French patients carrying a single mutated MEFV alleleSemantic proximity Read

P01-006 – MEFV mutation detection in Arabic patientsSemantic proximity Read

[Still disease with heterozygous MEFV mutation].Semantic proximity Read

Clinical and subclinical features and MEFV mutation distribution in of FMF patients’ siblingsSemantic proximity Read

EAS Consensus Panel statement on homozygous FH.Semantic proximity Read

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

The phenotype-genotype correlations of FMF patients: a single center study.Semantic proximity Read

Could familial Mediterranean fever gene mutations be related to PFAPA syndrome?Semantic proximity Read

Increasing Importance of Genotype–Phenotype Correlations Associated with Common and Rare MEFV Gene Mutations in FMF Patients in the Last Thirty YearsSemantic proximity Read