Epigenomic signature of adrenoleukodystrophy predicts compromised oligodendrocyte differentiation

Epigenomic changes may either cause disease or modulate its expressivity, adding a layer of complexity to mendelian diseases. X‐linked adrenoleukodystrophy (X‐ALD) is a rare neurometabolic condition exhibiting discordant phenotypes, ranging from a childhood cerebral inflammatory demyelination (cALD)...

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Dades bibliogràfiques
Publicat a:Brain Pathol
Autors principals: Schlüter, Agatha, Sandoval, Juan, Fourcade, Stéphane, Díaz‐Lagares, Angel, Ruiz, Montserrat, Casaccia, Patrizia, Esteller, Manel, Pujol, Aurora
Format: Artigo
Idioma:Inglês
Publicat: John Wiley and Sons Inc. 2018
Matèries:
Research Articles
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6857458/
https://ncbi.nlm.nih.gov/pubmed/29476661
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bpa.12595
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