Comparison of C26:0-carnitine and C26:0-lysophosphatidylcholine as diagnostic markers in dried blood spots from newborns and patients with adrenoleukodystrophy-Reference-Cited by-同舟云学术

Comparison of C26:0-carnitine and C26:0-lysophosphatidylcholine as diagnostic markers in dried blood spots from newborns and patients with adrenoleukodystrophy

Published:2017-12 Issue:4 Volume:122 Page:209-215
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Huffnagel Irene C.,van de Beek Malu-Clair,Showers Amanda L.,Orsini Joseph J.,Klouwer Femke C.C.,Dijkstra Inge M.E.,Schielen Peter C.,van Lenthe Henk,Wanders Ronald J.A.,Vaz Frédéric M.,Morrissey Mark A.,Engelen Marc,Kemp Stephan

Funder

European Leukodystrophy Association

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference39 articles.

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3. The human peroxisomal ABC half transporter ALDP functions as a homodimer and accepts acyl-CoA esters;van Roermund;FASEB J.,2008

4. Impaired very long-chain acyl-CoA beta-oxidation in human X-linked adrenoleukodystrophy fibroblasts is a direct consequence of ABCD1 transporter dysfunction;Wiesinger;J. Biol. Chem.,2013

5. Adrenoleukodystrophy: impaired oxidation of long chain fatty acids in cultured skin fibroblasts an adrenal cortex;Singh;Biochem. Biophys. Res. Commun.,1981

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