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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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Detalhes bibliográficos
Publicado no:JIMD Rep
Main Authors: Jones, Dylan E., Ricker, J. David, Geary, Laina M., Kosma, Dylan K., Ryan, Robert O.
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley & Sons, Inc. 2020
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7932859/
https://ncbi.nlm.nih.gov/pubmed/33728248
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jmd2.12185
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