Cardiovascular Research in Friedreich Ataxia: Unmet Needs and Opportunities

Friedreich Ataxia (FRDA) is an autosomal recessive disease in which a mitochondrial protein, frataxin, is severely decreased in its expression. In addition to progressive ataxia, patients with FRDA often develop a cardiomyopathy that can be hypertrophic. This cardiomyopathy is unlike the sarcomeric...

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Detalles Bibliográficos
Autor principal: Payne, R. Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
State-of-the-Art Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9831864/
https://www.ncbi.nlm.nih.gov/pubmed/36644283
http://dx.doi.org/10.1016/j.jacbts.2022.04.005

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9831864/
https://www.ncbi.nlm.nih.gov/pubmed/36644283
http://dx.doi.org/10.1016/j.jacbts.2022.04.005

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