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Volumn 69, Issue 1, 2000, Pages 64-68

Kearns-Sayre syndrome presenting as 2-oxoadipic aciduria

Author keywords

[No Author keywords available]

Indexed keywords

ACIDEMIA; ACIDURIA; ADULT; ARTICLE; CASE REPORT; FEMALE; GENE DELETION; GENOME; HEART BLOCK; HUMAN; KEARNS SAYRE SYNDROME; KETOACIDOSIS; OPHTHALMOPLEGIA; PRIORITY JOURNAL; RETINOPATHY; SOUTHERN BLOTTING; URINALYSIS;

EID: 0033955622     PISSN: 10967192     EISSN: None     Source Type: Journal    
DOI: 10.1006/mgme.1999.2946     Document Type: Article
Times cited : (13)

References (18)
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  • 3
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  • 5
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    • Tryptophan and lysine metabolism in alpha-aminoadipic aciduria
    • Fischer M H, Brown R R. Tryptophan and lysine metabolism in alpha-aminoadipic aciduria. Am J Med Genet. 5:1980;35-41.
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    • Fischer, M.H.1    Brown, R.R.2
  • 6
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    • Alpha-ketoadipic aciduria, a new inborn error of lysine metabolism: Biochemical studies
    • Przyrembel H, Bachmann D. Alpha-ketoadipic aciduria, a new inborn error of lysine metabolism: Biochemical studies. Clin Chim Acta. 58:1975;257-269.
    • (1975) Clin Chim Acta , vol.58 , pp. 257-269
    • Przyrembel, H.1    Bachmann, D.2
  • 7
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  • 8
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    • Automatic recording apparatus for use in chromatography of amino acids
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  • 9
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    • Purification of genomic DNA from human whole blood by isopropanol fractionation with concentrated NaI and SOS
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    • α-Ketoadipic aciduria: A description of a new metabolic error in lysine-tryptophan degradation
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.