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Table representation of search results timeline featuring number of search results per year.
| Year | Number of Results |
|---|---|
| 2020 | 1 |
| 2021 | 1 |
| 2026 | 0 |
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ETF dehydrogenase advances in molecular genetics and impact on treatment.
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 …
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