Murine model of triosephosphate isomerase deficiency with anemia and severe neuromuscular dysfunction

Triosephosphate isomerase deficiency (TPI Df) is a rare, aggressive genetic disease that typically affects young children and currently has no established treatment. TPI Df is characterized by hemolytic anemia, progressive neuromuscular degeneration, and a markedly reduced lifespan. The disease has...

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Detalles Bibliográficos
Autores principales: Myers, Tracey D., Ferguson, Carolyn, Gliniak, Eric, Homanics, Gregg E., Palladino, Michael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9673098/
https://www.ncbi.nlm.nih.gov/pubmed/36405628
http://dx.doi.org/10.1016/j.crneur.2022.100062

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9673098/
https://www.ncbi.nlm.nih.gov/pubmed/36405628
http://dx.doi.org/10.1016/j.crneur.2022.100062

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