ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency

Rikke K J Olsen, Simon E Olpin, Brage S Andresen, Zofia H Miedzybrodzka, Morteza Pourfarzam, Begoña Merinero, Frank E Frerman, Michael W Beresford, John C S Dean, Nanna Cornelius, Anders Oldfors, Elisabeth Holme, Niels Gregersen, Douglass M Turnbull, Andrew A M Morris

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

Fingeraftryk

Dyk ned i forskningsemnerne om 'ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency'. Sammen danner de et unikt fingeraftryk.

Biochemistry, Genetics and Molecular Biology

Pharmacology, Toxicology and Pharmaceutical Science

Neuroscience