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Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: Resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency
British Library Conference Proceedings | 1998| -
Bifunctional protein deficiency: Complementation within the same group suggesting differential enzyme defects and clues to the underlying basis
British Library Online Contents | 1998| -
D-Hydroxyacyl-CoA Dehydrogenase Deficiency: Identification of a New Peroxisomal Disorder with Implications for Other Disorders of beta-Oxidation
British Library Conference Proceedings | 1999| -
Identification of the 58 kDa SCPx (SCP2/Thiolase) as the main peroxisomal thiolase involved in branched-chain fatty acid oxidation: studies in mutant mice
British Library Online Contents | 1998| -
Proficiency testing in analytical chemistry, microbiology and laboratory medicine: working group discussions on current practice and future directions
British Library Online Contents | 2004| -
Identification of the 58 kDa SCPx (SCP2/Thiolase) as the main peroxisomal thiolase involved in branched-chain fatty acid oxidation: studies in mutant mice
British Library Conference Proceedings | 1998| -
Bifunctional protein deficiency: resolution of the underlying basis for the intragenic complementation using enzymological and immunological methods
British Library Online Contents | 1998| -
Peroxisomal bifunctional protein deficiency revisited: resolution of its true enzymatic and molecular basis
British Library Conference Proceedings | 1998| -
Peroxisomal bifunctional protein deficiency revisited: resolution of its true enzymatic and molecular basis
British Library Online Contents | 1998| -
Peroxisomal multifunctional -oxidation protein 2 deficiency: a new peroxisomal disorder and resolution of its molecular basis
British Library Online Contents | 1997| -
Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: Resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency
British Library Online Contents | 1998|
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