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]
Producer: 20011204Description: 714-22 p. digitalISSN:- 0014-2972
- 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
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Publication Type: Case Reports; Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
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