Gene Expression Analysis in gla-Mutant Zebrafish Reveals Enhanced Ca(2+) Signaling Similar to Fabry Disease

Fabry disease (FD) is an X-linked inborn metabolic disorder due to partial or complete lysosomal α-galactosidase A deficiency. FD is characterized by progressive renal insufficiency and cardio- and cerebrovascular involvement. Restricted access on Gb3-independent tissue injury experimental models ha...

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Detalles Bibliográficos
Autores principales: Elsaid, Hassan Osman Alhassan, Tjeldnes, Håkon, Rivedal, Mariell, Serre, Camille, Eikrem, Øystein, Svarstad, Einar, Tøndel, Camilla, Marti, Hans-Peter, Furriol, Jessica, Babickova, Janka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9820748/
https://www.ncbi.nlm.nih.gov/pubmed/36613802
http://dx.doi.org/10.3390/ijms24010358

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9820748/
https://www.ncbi.nlm.nih.gov/pubmed/36613802
http://dx.doi.org/10.3390/ijms24010358

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