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Volumn 78, Issue 2, 1998, Pages 192-194

Molecular diagnosis of alkaptonuria mutation by analysis of homogentisate 1,2 dioxygenase mRNA from urine and blood

Author keywords

Alkaptonuria; Diagnosis; Ectopic expression; RNA; Urine

Indexed keywords

HOMOGENTISIC ACID;

EID: 0032581046     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19980630)78:2<192::AID-AJMG20>3.0.CO;2-H     Document Type: Article
Times cited : (10)

References (12)
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    • Chomczynski, P.1    Sacchi, N.2
  • 4
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    • Molecular characterization of a gene encoding a homogentisate dioxygenase from Aspergillus nidulans and identification of its human and plant homologues
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    • Alkaptonuria
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    • (1989) "The Metabolic Basis of Inherited Diseases." 6th Ed. , pp. 775-790
    • La Du, B.N.1
  • 9
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    • The nature of the defect in tyrosine metabolism in alkaptonuria
    • La Du BN, Zannoni VG, Laster L, Seegmiller JE (1958): The nature of the defect in tyrosine metabolism in alkaptonuria. J Biol Chem 230:251-260.
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    • Access to a messenger RNA sequence or its protein product is not limited by tissue or species specificity
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  • 12
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    • Novel phenylketonuria mutation detected by analysis of ectopically transcribed phenylalanine hydroxylase mRNA from lymphoblast
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.