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Molecular Biomarkers for Adrenoleukodystrophy: An Unmet Need

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

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Detalles Bibliográficos
Autores principales: Honey, Madison I. J., Jaspers, Yorrick R. J., Engelen, Marc, Kemp, Stephan, Huffnagel, Irene C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8699919/
https://www.ncbi.nlm.nih.gov/pubmed/34943935
http://dx.doi.org/10.3390/cells10123427

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