Abcd2 Is a Strong Modifier of the Metabolic Impairments in Peritoneal Macrophages of Abcd1-Deficient Mice

The inherited peroxisomal disorder X-linked adrenoleukodystrophy (X-ALD), associated with neurodegeneration and inflammatory cerebral demyelination, is caused by mutations in the ABCD1 gene encoding the peroxisomal ATP-binding cassette (ABC) transporter ABCD1 (ALDP). ABCD1 transports CoA-esters of v...

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Bibliografski detalji
Glavni autori: Muneer, Zahid, Wiesinger, Christoph, Voigtländer, Till, Werner, Hauke B., Berger, Johannes, Forss-Petter, Sonja
Format: Artigo
Jezik:Inglês
Izdano: Public Library of Science 2014
Teme:
Research Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4177892/
https://ncbi.nlm.nih.gov/pubmed/25255441
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0108655
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