Proteomic analysis unveils Gb3-independent alterations and mitochondrial dysfunction in a gla -/- zebrafish model of Fabry disease.
Hassan Osman Alhassan ElsaidMariell RivedalEleni SkandalouEinar SvarstadCamilla TøndelEven BirkelandØystein EikremJanka BabickovaHans-Peter MartiJessica FurriolPublished in: Journal of translational medicine (2023)
mutant model proves valuable in elucidating these mechanisms and may contribute significantly to advancing our knowledge of this disorder.