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Volumn 40, Issue 10, 1997, Pages 1896-1898

Azathioprine-induced severe pancytopenia due to a homozygous two-point mutation of the thiopurine methyltransferase gene in a patient with juvenile HLA-B27-associated spondylarthritis

Author keywords

[No Author keywords available]

Indexed keywords

AMPHOTERICIN; AZATHIOPRINE; COTRIMOXAZOLE; DICLOFENAC; GRANULOCYTE COLONY STIMULATING FACTOR; HLA B27 ANTIGEN; NONSTEROID ANTIINFLAMMATORY AGENT; STEROID; THIOPURINE METHYLTRANSFERASE;

EID: 0030871031     PISSN: 00043591     EISSN: None     Source Type: Journal    
DOI: 10.1002/art.1780401026     Document Type: Article
Times cited : (83)

References (14)
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  • 2
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  • 4
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    • Tai HL, Krynetsky EY, Yates CR, Loennechen T, Fessing MY, Krynetskaia NF, Evans WE: Thiopurinc S-methyltransferase deficiency: two nucleotide transitions define the most prevalent mutant allele associated with loss of catalytic activity in Caucasians. Am J Hum Genet 58:694-702, 1996
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  • 8
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  • 11
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.