The Downregulation of c19orf12 Negatively Affects Neuronal and Musculature Development in Zebrafish Embryos

Mitochondrial membrane Protein Associated Neurodegeneration (MPAN) is a rare genetic disorder due to mutations in C19orf12 gene. In most cases, the disorder is transmitted as an autosomal recessive trait and the main clinical features are progressive spastic para/tetraparesis, dystonia, motor axonal...

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Detalles Bibliográficos
Autores principales: Mignani, Luca, Zizioli, Daniela, Borsani, Giuseppe, Monti, Eugenio, Finazzi, Dario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7785858/
https://www.ncbi.nlm.nih.gov/pubmed/33425903
http://dx.doi.org/10.3389/fcell.2020.596069

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7785858/
https://www.ncbi.nlm.nih.gov/pubmed/33425903
http://dx.doi.org/10.3389/fcell.2020.596069

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