Phytanic acid alpha-oxidation: accumulation of 2-hydroxyphytanic acid and absence of 2-oxophytanic acid in plasma from patients with peroxisomal disorders.-Reference-Cited by-同舟云学术

Phytanic acid alpha-oxidation: accumulation of 2-hydroxyphytanic acid and absence of 2-oxophytanic acid in plasma from patients with peroxisomal disorders.

Published:1992-10 Issue:10 Volume:33 Page:1449-1457
ISSN:0022-2275
Container-title:Journal of Lipid Research
language:en
Short-container-title:Journal of Lipid Research

Author:

ten Brink HJ,Schor DS,Kok RM,Poll-The BT,Wanders RJ,Jakobs C

Publisher

Elsevier BV

Subject

Cell Biology,Endocrinology,Biochemistry

Reference21 articles.

1. Refsum disease;Steinberg,1989

2. Peroxisomal disorders in neurology;Wanders;J. Neurol. Sci.,1988

3. Pristanic acid and phytanic acid in plasma from patients with peroxisomal disorders: stable isotope dilution analysis with electron capture negative ion mass fragmentography;ten Brink;J. Lipid Res.,1992

4. Refsum's disease. Nature of the enzyme defect;Steinberg;Science.,1967

5. Refsum's disease: characterization of the enzyme defect in cell culture;Herndon;J. Clin. Invest.,1969

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