HSD10 disease: clinical consequences of mutations in the HSD17B10 gene (Q37962802)

26 August 2017

title

HSD10 disease: clinical consequences of mutations in the HSD17B10 gene (English)

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26 August 2017

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Johannes Zschocke

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26 August 2017

language of work or name

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30 November 2011

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Journal of Inherited Metabolic Disease

26 August 2017

published in

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26 August 2017

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26 August 2017

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26 August 2017

page(s)

81-89

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Biochemical characterization and crystal structure determination of human heart short chain L-3-hydroxyacyl-CoA dehydrogenase provide insights into catalytic mechanism

26 August 2017

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2-Methyl-3-Hydroxybutyryl-CoA Dehydrogenase Deficiency Is Caused by Mutations in the HADH2 Gene

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A non-enzymatic function of 17beta-hydroxysteroid dehydrogenase type 10 is required for mitochondrial integrity and cell survival

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12 December 2020

Intrinsic alcohol dehydrogenase and hydroxysteroid dehydrogenase activities of human mitochondrial short-chain L-3-hydroxyacyl-CoA dehydrogenase

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12 December 2020

Newborn screening: toward a uniform screening panel and system

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12 December 2020

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12 December 2020

Purification and Properties of a Specific Escherichia coli Ribonuclease which Cleaves a Tyrosine Transfer Ribonucleic Acid Precursor

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Short-Chain 3-Hydroxy-2-methylacyl-CoA Dehydrogenase from Rat Liver: Purification and Characterization of a Novel Enzyme of Isoleucine Metabolism

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12 December 2020

10.1007/S10545-011-9415-4

Identifiers

DOI

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26 August 2017

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