[Still disease with heterozygous MEFV mutation]
Presse Med
.
2015 Sep;44(9):970-1.
doi: 10.1016/j.lpm.2015.04.028.
Epub 2015 Jun 10.
[Article in French]
Authors
Aurianne Mallick
1
,
Renaud Felten
1
,
Elsa Widawski
1
,
Antoine Mahé
2
,
Laurent Messer
3
Affiliations
1
Hôpitaux civils de Colmar, service de rhumatologie, 68000 Colmar, France.
2
Hôpitaux civils de Colmar, service de dermatologie, 68000 Colmar, France.
3
Hôpitaux civils de Colmar, service de rhumatologie, 68000 Colmar, France. Electronic address: laurentmesser@yahoo.fr.
PMID:
26071026
DOI:
10.1016/j.lpm.2015.04.028
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Adult
Arthritis, Juvenile / diagnosis*
Arthritis, Juvenile / genetics
Cytoskeletal Proteins / genetics*
Heterozygote
Humans
Male
Mutation
Pedigree
Pyrin
Substances
Cytoskeletal Proteins
MEFV protein, human
Pyrin