Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),General Medicine
Reference35 articles.
1. Frerman FE, Goodman SI (1985) Deficiency of electron transfer flavoprotein or electron transfer flavoprotein:ubiquinone oxidoreductase in glutaric acidemia type II fibroblasts. Proc Natl Acad Sci 82:4517–4520. https://doi.org/10.1073/pnas.82.13.4517
2. Prasun P (1993) Multiple acyl-CoA dehydrogenase deficiency. In: Adam MP, Ardinger HH, Pagon RA, et al (eds) GeneReviews®. University of Washington, Seattle, WA. https://www.ncbi.nlm.nih.gov/books/NBK558236/
3. Yıldız Y, Talim B, Haliloglu G et al (2019) Determinants of riboflavin responsiveness in multiple Acyl-CoA dehydrogenase deficiency. Pediatr Neurol 99:69–75. https://doi.org/10.1016/j.pediatrneurol.2019.06.015
4. Zhou D, Ye M, Hu Z et al (2021) Screening of multiple acyl-CoA dehydrogenase deficiency in newborns and follow-up of patients. Zhejiang Da Xue Xue Bao Yi Xue Ban 50:454–462. https://doi.org/10.3724/zdxbyxb-2021-0261
5. Ohkuma A, Noguchi S, Sugie H et al (2009) Clinical and genetic analysis of lipid storage myopathies. Muscle Nerve 39:333–342. https://doi.org/10.1002/mus.21167
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