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Any multiple acyl-CoA dehydrogenase deficiency in which the cause of the disease is a mutation in the ETFB gene.
No clinical trials have been registered for glutaric acidemia IIb.
3 publications have been identified in PubMed for glutaric acidemia IIb. Research spans Review / Meta-Analysis (33%), Case Report / Case Series (33%), and Basic Science / Preclinical (33%).
Martino S (2024). [PMID: 39273584](https://pubmed.ncbi.nlm.nih.gov/39273584/). *Int J Mol Sci*. [Case Report / Case Series]
Seyedtaghia MR (2024). [PMID: 38967380](https://pubmed.ncbi.nlm.nih.gov/38967380/). *Mol Genet Genomic Med*. [Review / Meta-Analysis]
Demetriou K (2024). [PMID: 38941880](https://pubmed.ncbi.nlm.nih.gov/38941880/). *Mol Genet Metab*. [Basic Science / Preclinical]
Data assembled from 2 of 12 sources · Last updated Sep 19, 2026, 2:52 PM UTC