The Inflammatory Response in Acyl-CoA Oxidase 1 Deficiency (Pseudoneonatal Adrenoleukodystrophy)

Autor: Pierre Andreoletti, Stéphane Mandard, Aurore Vluggens, Gérard Lizard, Sander Kersten, Janardan K. Reddy, H. I. El Hajj, Kévin Ragot, Ronald J.A. Wanders, H. R. Waterham, Mustapha Cherkaoui-Malki

Publikováno v: Endocrinology, 153(6), 2568-2575. The Endocrine Society
Endocrinology
Endocrinology, Endocrine Society, 2012, 153 (6), pp.2568-75. 〈10.1210/en.2012-1137〉
Endocrinology, Endocrine Society, 2012, 153 (6), pp.2568-75. ⟨10.1210/en.2012-1137⟩
Endocrinology, 153(6), 2568-2575
Endocrinology 153 (2012) 6

Among several peroxisomal neurodegenerative disorders, the pseudoneonatal adrenoleukodystrophy (P-NALD) is characterized by the acyl-coenzyme A oxidase 1 (ACOX1) deficiency, which leads to the accumulation of very-long-chain fatty acids ( VLCFA) and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b25c8f0010ebbc23f73a7fe631931ebf
https://pure.amc.nl/en/publications/the-inflammatory-response-in-acylcoa-oxidase-1-deficiency-pseudoneonatal-adrenoleukodystrophy(7bd25523-b244-427f-ad1d-aaed82029c73).html