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Any multiple acyl-CoA dehydrogenase deficiency in which the cause of the disease is a mutation in the ETFA gene.
No clinical trials have been registered for glutaric acidemia IIa.
4 publications have been identified in PubMed for glutaric acidemia IIa. Research spans Case Report / Case Series (50%), Review / Meta-Analysis (25%), and Basic Science / Preclinical (25%).
Parvini F (2025). [PMID: 41254678](https://pubmed.ncbi.nlm.nih.gov/41254678/). *Orphanet J Rare Dis*. [Case Report / Case Series]
Demetriou K (2024). [PMID: 38941880](https://pubmed.ncbi.nlm.nih.gov/38941880/). *Mol Genet Metab*. [Basic Science / Preclinical]
Seyedtaghia MR (2024). [PMID: 38967380](https://pubmed.ncbi.nlm.nih.gov/38967380/). *Mol Genet Genomic Med*. [Review / Meta-Analysis]
Martino S (2024). [PMID: 39273584](https://pubmed.ncbi.nlm.nih.gov/39273584/). *Int J Mol Sci*. [Case Report / Case Series]
Data assembled from 2 of 12 sources · Last updated Sep 19, 2026, 6:45 AM UTC