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Mutant holocarboxylase synthetase: evidence for the enzyme defect in early infantile biotin-responsive multiple carboxylase deficiency.

Data up to Jan 2025

Published1981
Citations150
References17

Total Citations Per Year

Abstract

References (17)

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Biotin-Responsive Carboxylase Deficiency Associated with Subnormal Plasma and Urinary Biotin

1981 • 101 citations

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1981 • 94 citations

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1979 • 74 citations

Propionyl-CoA Carboxylase Deficiency in a Patient with Biotin-responsive 3-Methylcrotonylglycinuria

1977 • 72 citations

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1962 • 56 citations

Beta-methylcrotonic aciduria associated with lactic acidosis

1976 • 51 citations

Holocarboxylase synthetase deficiency: A biotin-responsive organic acidemia

1980 • 49 citations

The Enzymatic Synthesis of Propionyl Coenzyme A Holocarboxylase from d-Biotinyl 5'-Adenylate and the Apocarboxylase

1965 • 32 citations

[77] Propionyl CoA carboxylase from pig heart

1962 • 13 citations

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1981 • 5 citations

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Mutant holocarboxylase synthetase: evidence for the enzyme defect in early infantile… (1981) – Journal of Clinical Investigation | Metascience Observatory Explorer