Dysregulated DNA methylation in the pathogenesis of Fabry disease

Fabry disease is an X-linked lysosomal storage disorder caused by a deficiency of α-galactosidase A and subsequent accumulation of glycosphingolipids with terminal α-D-galactosyl residues. The molecular process through which this abnormal metabolism of glycosphingolipids causes multisystem dysfuncti...

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Detalles Bibliográficos
Autores principales: Shen, Jin-Song, Balaji, Uthra, Shigeyasu, Kunitoshi, Okugawa, Yoshinaga, Jabbarzadeh-Tabrizi, Siamak, Day, Taniqua S., Arning, Erland, Marshall, John, Cheng, Seng H., Gu, Jinghua, Schiffmann, Raphael, Bottiglieri, Teodoro, Goel, Ajay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9519376/
https://www.ncbi.nlm.nih.gov/pubmed/36186841
http://dx.doi.org/10.1016/j.ymgmr.2022.100919

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9519376/
https://www.ncbi.nlm.nih.gov/pubmed/36186841
http://dx.doi.org/10.1016/j.ymgmr.2022.100919

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