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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Detalles Bibliográficos
Autores principales: Schlüter, Agatha, Sandoval, Juan, Fourcade, Stéphane, Díaz‐Lagares, Angel, Ruiz, Montserrat, Casaccia, Patrizia, Esteller, Manel, Pujol, Aurora
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6857458/
https://www.ncbi.nlm.nih.gov/pubmed/29476661
http://dx.doi.org/10.1111/bpa.12595

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6857458/
https://www.ncbi.nlm.nih.gov/pubmed/29476661
http://dx.doi.org/10.1111/bpa.12595

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