Mevalonate kinase deficiency and Dutch type periodic fever

Clinical and Experimental Rheumatology

Volumn 18, Issue 4, 2000, Pages 525-532

  Frenkel, J ^a   Houten, S M ^a   Waterham, H R ^a   Wanders, R J A ^a   Rijkers, G T ^a   Kimpen, J L L ^a   Duran, R ^a   Poll The, B T ^a   Kuis, W ^a  

^a UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

Author keywords

Familial Mediterranean fever; Fever; Hypergammaglobulinemia; IgD; Mevalonate kinase; Mevalonic acid; Periodicity

Indexed keywords

ACUTE PHASE PROTEIN; MEVALONIC ACID; PHOSPHOTRANSFERASE;

ACIDURIA; AUTOSOMAL RECESSIVE DISORDER; CLINICAL FEATURE; ENZYME DEFICIENCY; FACE DYSMORPHIA; FEVER; GRANULOCYTOSIS; HETEROZYGOSITY; HYPERIMMUNOGLOBULINEMIA; MENTAL DEFICIENCY; MISSENSE MUTATION; PHENOTYPE; PRIORITY JOURNAL; REVIEW;

CHILD; FAMILIAL MEDITERRANEAN FEVER; HUMANS; MUTATION, MISSENSE; PHOSPHOTRANSFERASES (ALCOHOL GROUP ACCEPTOR);

EID: 0033861821     PISSN: 0392856X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

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