Art
J-GLOBAL ID：200902299466285762
Reference number：04A0364802
E148Q/M694I Mutation in 3 Japanese Patients with Familial Mediterranean Fever
家族性地中海熱の日本人3患者におけるE148Q/M694I変異
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Material：
Volume：
79
Issue：
3
Page：
235-237
Publication year：
Apr. 2004
JST Material Number：
F0888A
ISSN：
0925-5710
CODEN：
IJHEEY
Document type：
Article
Article type：
原著論文
Country of issue：
Germany, Federal Republic of (DEU)
Language：
ENGLISH (EN)
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Semi thesaurus term：
Thesaurus term/Semi thesaurus term
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JST classification (2)：
JST classification
Category name(code) classified by JST.
Congenital diseases,deformities in general.
, Molecular genetics in general
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Reference (13)：
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The International FMF Consortium. Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever. Cell. 1997, 90, 797-807
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The French FMF Consortium. A candidate gene for familial Mediter-ranean fever. Nat Genet. 1997, 17, 25-31
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SOHAR, E. Familial Mediterranean fever : a survey of 470 cases and review of the literature. Am J Med. 1967, 43, 227-253
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SHINOZAKI, K. Familial Mediterranean fever in 2 Japanese families. J Rheumatol. 2002, 29, 1324-1325
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TOMIYAMA, N. End-stage renal disease associated with familial Mediterranean fever. Intern Med. 2002, 41, 221-224
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