Characterization of mutant holocarboxylase synthetase (HCS): A K(m) for biotin was not elevated in a patient with HCS deficiency

Pediatric Research

Volumn 42, Issue 6, 1997, Pages 849-854

  Aoki, Yoko ^a   Suzuki, Yoichi ^a   Li, Xue ^a   Sakamoto, Osamu ^a   Chikaoka, Hiroshi ^b   Takita, Seiji ^b   Narisawa, Kuniaki ^a  

^a TOHOKU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b SHOWA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CARBOXYLASE; SYNTHETASE;

ARTICLE; CARBOXYLATION; CASE REPORT; CELL TRANSFORMATION; CHILD; DISORDERS OF CARBOHYDRATE METABOLISM; ENZYME ACTIVITY; ENZYME ANALYSIS; ENZYME DEFICIENCY; FATTY ACID SYNTHESIS; FEMALE; FIBROBLAST; GENE MUTATION; HUMAN; KETOACIDOSIS; ONSET AGE; PRIORITY JOURNAL;

EID: 0030702915     PISSN: 00313998     EISSN: None     Source Type: Journal    
DOI: 10.1203/00006450-199712000-00021     Document Type: Article

References (26)

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