Molecular Biomarkers for Adrenoleukodystrophy: An Unmet Need

X-linked adrenoleukodystrophy (ALD) is an inherited progressive neurometabolic disease caused by mutations in the <i>ABCD1</i> gene and the accumulation of very long-chain fatty acids in plasma and tissues. Patients present with heterogeneous clinical manifestations which can include adr...

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Bibliographic Details
Published in:Cells
Main Authors: Madison I. J. Honey, Yorrick R. J. Jaspers, Marc Engelen, Stephan Kemp, Irene C. Huffnagel
Format: Article
Language:English
Published: MDPI AG 2021-12-01
Subjects:
biomarkers
biobank
cerebral demyelination
myelopathy
newborn screening
peroxisome
Online Access:https://www.mdpi.com/2073-4409/10/12/3427

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https://www.mdpi.com/2073-4409/10/12/3427

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