A comparative study on riboflavin responsive multiple acyl-CoA dehydrogenation deficiency due to variants in FLAD1 and ETFDH gene
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Springer Science and Business Media LLC
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https://www.nature.com/articles/s10038-023-01216-3.pdf
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4. Tein I, Elpeleg O, Ben-Zeev B, Korman SH, Lossos A, Lev D, et al. Short-chain acyl-CoA dehydrogenase gene mutation (c.319C>T) presents with clinical heterogeneity and is candidate founder mutation in individuals of Ashkenazi Jewish origin. Mol Genet Metab. 2008;93:179–89.
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