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Article

Development and characterization of a mouse model for Acad9 deficiency.

Molecular genetics and metabolism - 1 Jan 2000

Sinsheimer Andrew, Mohsen Al-Walid, Bloom Kailyn, Karunanidhi Anuradha, Bharathi Sivakama, Wu Yijen L, Schiff Manuel, Wang Yudong, Goetzman Eric S, Ghaloul-Gonzalez Lina, Vockley Jerry

Abstract excerpt

Acyl CoA Dehydrogenase 9 (ACAD9) is a member of the family of flavoenzymes that catalyze the dehydrogenation of acyl-CoAs to 2,3 enoyl-CoAs in mitochondrial fatty acid oxidation (FAO). Inborn errors of metabolism of all family members, including ACAD9, have been described in humans, and represent significant causes of morbidity and mortality particularly in children. ACAD9 deficiency leads to a combined defect in...

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Source

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Identifiers

PMID: 34556413
DOI: 10.1016/j.ymgme.2021.09.002
PMCID: PMC8588265

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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