Absence of hepatic molybdenum cofactor: an inborn error of metabolism leading to a combined deficiency of sulphite oxidase and xanthine dehydrogenase.
about
Molybdenum: an essential trace element.Molybdenum cofactor biosynthesis in humans. Identification of two complementation groups of cofactor-deficient patients and preliminary characterization of a diffusible molybdopterin precursor.Involvement of chlA, E, M, and N loci in Escherichia coli molybdopterin biosynthesisBiogenesis of molybdenum cofactors.Genetic trace metal disturbances.Dysmorphic syndromes with demonstrable biochemical abnormalities.Sulfite hypersensitivity. A critical review.Absence of hepatic molybdenum cofactor. An inborn error of metabolism associated with lens dislocation.
P2860
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P2860
Absence of hepatic molybdenum cofactor: an inborn error of metabolism leading to a combined deficiency of sulphite oxidase and xanthine dehydrogenase.
description
1983 nî lūn-bûn
@nan
1983年の論文
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1983年学术文章
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1983年学术文章
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1983年学术文章
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1983年学术文章
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1983年学术文章
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1983年学术文章
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1983年學術文章
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1983年學術文章
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name
Absence of hepatic molybdenum ...... se and xanthine dehydrogenase.
@en
Absence of hepatic molybdenum ...... se and xanthine dehydrogenase.
@nl
type
label
Absence of hepatic molybdenum ...... se and xanthine dehydrogenase.
@en
Absence of hepatic molybdenum ...... se and xanthine dehydrogenase.
@nl
prefLabel
Absence of hepatic molybdenum ...... se and xanthine dehydrogenase.
@en
Absence of hepatic molybdenum ...... se and xanthine dehydrogenase.
@nl
P2093
P356
P1476
Absence of hepatic molybdenum ...... se and xanthine dehydrogenase.
@en
P2093
C Charpentier
F A Beemer
J L Johnson
J M Saudubray
K V Rajagopalan
S K Wadman
P2888
P356
10.1007/BF01811328
P478
P577
1983-01-01T00:00:00Z