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Two forms of biotin-responsive multiple carboxylase deficiency.

作者信息

Sweetman L

出版信息

J Inherit Metab Dis. 1981;4(2):53-4. doi: 10.1007/BF02263587.

Abstract

Biotin-responsive multiple carboxylase deficiencies are classified into early and late forms. The early form showed higher urinary excretion of 3-hydroxyisovalerate and 3-hydroxypropionate than the late form and was associated with normal plasma biotin concentrations. It is proposed that holocarboxylase synthetase and intestinal biotin absorption are defective in the early and late forms respectively.

摘要

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