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Sulfite Alters the Mitochondrial Network in Molybdenum Cofactor Deficiency

Molybdenum cofactor deficiency (MoCD) is an autosomal recessive disorder belonging to the large family of inborn errors in metabolism. Patients typically present with encephalopathy and seizures early after birth and develop severe neurodegeneration within the first few weeks of life. The main patho...

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Detalles Bibliográficos
Autores principales: Mellis, Anna-Theresa, Roeper, Juliane, Misko, Albert L., Kohl, Joshua, Schwarz, Guenter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7817995/
https://www.ncbi.nlm.nih.gov/pubmed/33488670
http://dx.doi.org/10.3389/fgene.2020.594828