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Volumn 64, Issue 4, 1999, Pages 939-942

The genetic basis for periodic fever

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME 16P; EDITORIAL; FEVER; GENE MUTATION; GENETIC LINKAGE; HUMAN; HYPERGAMMAGLOBULINEMIA; PRIORITY JOURNAL; RECURRENT DISEASE;

EID: 0033361917     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302347     Document Type: Editorial
Times cited : (8)

References (13)
  • 1
    • 0030875991 scopus 로고    scopus 로고
    • Genetic linkage study of familial Mediterranean fever (FMF) to 16p13.3 and evidence for genetic heterogeneity in the Turkish population
    • AN Akarsu U Saatci S Ozen A Bakkaloglu N Besbas S Mansoor Genetic linkage study of familial Mediterranean fever (FMF) to 16p13.3 and evidence for genetic heterogeneity in the Turkish population J Med Genet 34 1997 573 578
    • (1997) J Med Genet , vol.34 , pp. 573-578
    • Akarsu, AN1    Saatci, U2    Ozen, S3    Bakkaloglu, A4    Besbas, N5    Mansoor, S6
  • 2
    • 18244429610 scopus 로고    scopus 로고
    • Mutation and haplotype studies in familial Mediterranean fever reveal new ancestral relationships and evidence for a high carrier frequency with reduced penetrance in the Ashkenazi Jewish population
    • I Aksentijevich Y Torosyan J Samuels M Centola E Pras JJ Chae C Oddoux Mutation and haplotype studies in familial Mediterranean fever reveal new ancestral relationships and evidence for a high carrier frequency with reduced penetrance in the Ashkenazi Jewish population Am J Hum Genet 64 1999 949 962 (in this issue)
    • (1999) Am J Hum Genet , vol.64 , pp. 949-962
    • Aksentijevich, I1    Torosyan, Y2    Samuels, J3    Centola, M4    Pras, E5    Chae, JJ6    Oddoux, C7
  • 3
    • 7344255810 scopus 로고    scopus 로고
    • Non-founder mutations in the MEFV gene establish this gene as the cause of familial Mediterranean fever (FMF)
    • A Bernot C da Silva J-L Petit C Cruaud C Caloustian V Castet M Ahmed-Arab Non-founder mutations in the MEFV gene establish this gene as the cause of familial Mediterranean fever (FMF) Hum Mol Genet 7 1998 1317 1325
    • (1998) Hum Mol Genet , vol.7 , pp. 1317-1325
    • Bernot, A1    da Silva, C2    Petit, J-L3    Cruaud, C4    Caloustian, C5    Castet, V6    Ahmed-Arab, M7
  • 5
    • 16944365196 scopus 로고    scopus 로고
    • A candidate gene for familial Mediterranean fever
    • French FMF Consortium A candidate gene for familial Mediterranean fever Nat Genet 17 1997 25 31
    • (1997) Nat Genet , vol.17 , pp. 25-31
    • French FMF Consortium1
  • 7
    • 0030745449 scopus 로고    scopus 로고
    • Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever
    • International FMF Consortium, The Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever Cell 90 1997 797 807
    • (1997) Cell , vol.90 , pp. 797-807
    • International FMF Consortium, The,1
  • 12
    • 0029816014 scopus 로고    scopus 로고
    • Exhaustive mutation scanning by fluorescence-assisted mismatch analysis discloses new genotype-phenotype correlations in angioedema
    • E Verpy M Biasotto M Brai G Misiano T Meo M Tosi Exhaustive mutation scanning by fluorescence-assisted mismatch analysis discloses new genotype-phenotype correlations in angioedema Am J Hum Genet 59 1996 308 319
    • (1996) Am J Hum Genet , vol.59 , pp. 308-319
    • Verpy, E1    Biasotto, M2    Brai, M3    Misiano, G4    Meo, T5    Tosi, M6
  • 13
    • 0027278997 scopus 로고
    • Two distinct mutations in a single dystrophin gene: identification of an altered splice-site as the primary Becker muscular dystrophy mutation
    • SD Wilton RD Johnsen JR Pedretti NG Laing Two distinct mutations in a single dystrophin gene: identification of an altered splice-site as the primary Becker muscular dystrophy mutation Am J Med Genet 46 1993 563 569
    • (1993) Am J Med Genet , vol.46 , pp. 563-569
    • Wilton, SD1    Johnsen, RD2    Pedretti, JR3    Laing, NG4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.