Autosomal dominant familial Mediterranean fever in Northern European Caucasians associated with deletion of p.M694 residue—a case series and genetic exploration-Reference-Cited by-同舟云学术

Autosomal dominant familial Mediterranean fever in Northern European Caucasians associated with deletion of p.M694 residue—a case series and genetic exploration

Published:2016-05-05 Issue:2 Volume:56 Page:209-213
ISSN:1462-0324
Container-title:Rheumatology
language:en
Short-container-title:Rheumatology

Author:

Rowczenio Dorota M.,Iancu Daniela S.,Trojer Hadija,Gilbertson Janet A.,Gillmore Julian D.,Wechalekar Ashutosh D.,Tekman Mehmet,Stanescu Horia C.,Kleta Robert,Lane Thirusha,Hawkins Philip N.,Lachmann Helen J.

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

Link

http://academic.oup.com/rheumatology/article-pdf/56/2/209/9951656/kew058.pdf

Reference19 articles.

1. A candidate gene for familial Mediterranean fever

2. Infevers: An evolving mutation database for auto-inflammatory syndromes

3. The spectrum of Familial Mediterranean Fever (FMF) mutations

4. Genotype–phenotype correlation in a large group of Turkish patients with familial Mediterranean fever: evidence for mutation-independent amyloidosis

5. Phenotype–genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosis

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