Fibroblast studies documenting a case of peroxisomal 2-methylacyl-CoA racemase deficiency: possible link between racemase deficiency and malabsorption and vitamin K deficiency.
Van Veldhoven, P P
Fibroblast studies documenting a case of peroxisomal 2-methylacyl-CoA racemase deficiency: possible link between racemase deficiency and malabsorption and vitamin K deficiency. [electronic resource] - European journal of clinical investigation Aug 2001 - 714-22 p. digital
Publication Type: Case Reports; Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
0014-2972
10.1046/j.1365-2362.2001.00877.x doi
Cells, Cultured
Fatty Acids--chemical synthesis
Female
Fibroblasts--enzymology
Humans
Infant, Newborn
Isomerism
Malabsorption Syndromes--etiology
Oxidation-Reduction
Palmitic Acids--chemical synthesis
Peroxisomal Disorders--enzymology
Peroxisomes--enzymology
Racemases and Epimerases--deficiency
Skin--cytology
Vitamin K Deficiency--etiology
Fibroblast studies documenting a case of peroxisomal 2-methylacyl-CoA racemase deficiency: possible link between racemase deficiency and malabsorption and vitamin K deficiency. [electronic resource] - European journal of clinical investigation Aug 2001 - 714-22 p. digital
Publication Type: Case Reports; Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
0014-2972
10.1046/j.1365-2362.2001.00877.x doi
Cells, Cultured
Fatty Acids--chemical synthesis
Female
Fibroblasts--enzymology
Humans
Infant, Newborn
Isomerism
Malabsorption Syndromes--etiology
Oxidation-Reduction
Palmitic Acids--chemical synthesis
Peroxisomal Disorders--enzymology
Peroxisomes--enzymology
Racemases and Epimerases--deficiency
Skin--cytology
Vitamin K Deficiency--etiology