Isomerization of trans‐3‐methylglutaconic acid

3‐Methylglutaconic (3MGC) aciduria is a common phenotypic feature of a growing number of inborn errors of metabolism. “Primary” 3MGC aciduria is caused by deficiencies in leucine pathway enzymes while “secondary” 3MGC aciduria results from inborn errors of metabolism that impact mitochondrial energy...

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Detalles Bibliográficos
Autores principales: Jones, Dylan E., Ricker, J. David, Geary, Laina M., Kosma, Dylan K., Ryan, Robert O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Research Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7932859/
https://www.ncbi.nlm.nih.gov/pubmed/33728248
http://dx.doi.org/10.1002/jmd2.12185

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7932859/
https://www.ncbi.nlm.nih.gov/pubmed/33728248
http://dx.doi.org/10.1002/jmd2.12185

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