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ETF dehydrogenase advances in molecular genetics and impact on treatment.
Missaglia S, Tavian D, Angelini C. Missaglia S, et al. Crit Rev Biochem Mol Biol. 2021 Aug;56(4):360-372. doi: 10.1080/10409238.2021.1908952. Epub 2021 Apr 7. Crit Rev Biochem Mol Biol. 2021. PMID: 33823724 Review.
ETF-QO mutations are often associated with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (RR-MADD, OMIM#231680), a multisystem genetic disease characterized by various clinical manifestations with different degrees of severity. In this r
ETF-QO mutations are often associated with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (RR-MADD, O …
Riboflavin Deficiency-Implications for General Human Health and Inborn Errors of Metabolism.
Mosegaard S, Dipace G, Bross P, Carlsen J, Gregersen N, Olsen RKJ. Mosegaard S, et al. Int J Mol Sci. 2020 May 28;21(11):3847. doi: 10.3390/ijms21113847. Int J Mol Sci. 2020. PMID: 32481712 Free PMC article. Review.
A latent subclinical riboflavin deficiency can result in a significant clinical phenotype when combined with inborn genetic disturbances or environmental and physiological factors like infections, exercise, diet, aging and pregnancy. ...Numerous inborn errors of fla …
A latent subclinical riboflavin deficiency can result in a significant clinical phenotype when combined with inborn genetic di …