Concepedia

Publication | Closed Access

An intronic variation in SLC52A1 causes exon skipping and transient riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency

DOI

56

Citations

27

References

2017

Year

Signe Mosegaard, Gitte Hoffmann Bruun, Karen Freund Flyvbjerg, Yngve Thomas Bliksrud, Niels Gregersen, Maja Dembić, Ellen Annexstad, Trine Tangeraas, Rikke Katrine Jentoft Olsen, Brage Storstein Andresen
Molecular Genetics and Metabolism

References

YearCitations

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