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Volumn 85, Issue 3, 2000, Pages 1320-1322

A heterozygous deletion of the autoimmune regulator (AIRE1) gene, autoimmune thyroid disease, and type 1 diabetes: No evidence for association

Author keywords

[No Author keywords available]

Indexed keywords

ADRENAL INSUFFICIENCY; AUTOIMMUNE DISEASE; CANDIDIASIS; CHROMOSOME 21Q; CONTROLLED STUDY; GENE DELETION; GENE MUTATION; GENETIC SUSCEPTIBILITY; GRAVES DISEASE; HETEROZYGOSITY; HUMAN; HYPOTHYROIDISM; INSULIN DEPENDENT DIABETES MELLITUS; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; REGULATOR GENE; REVIEW; THYROID DISEASE;

EID: 0034454508     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jc.85.3.1320     Document Type: Review
Times cited : (48)

References (26)
  • 17
    • 0346599403 scopus 로고    scopus 로고
    • An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zincfinger domains. Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy
    • (1997) Nat Genet , vol.17 , pp. 399-403
  • 20
    • 15144361587 scopus 로고    scopus 로고
    • Linkage disequilibrium between the human leukocyte antigen class II region of the major histocompatibility complex and Graves' disease: Replication using a population case control and family-based study
    • (1998) J Clin Endocrinol Metab , vol.83 , pp. 3394-3397
    • Heward, J.M.1    Allahabadia, A.2    Daykin, J.3
  • 22
    • 0033082240 scopus 로고    scopus 로고
    • From genome to aetiology in a multifactorial disease, type 1 diabetes
    • (1999) Bioassays , vol.21 , pp. 164-174
    • Todd, J.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.