@article{f95d6b4a8af1478e988922d04ff983a2,
title = "Patient with multiple acyl-CoA dehydrogenation deficiency disease and FLAD1 mutations benefits from riboflavin therapy",
keywords = "Genetics, Neuromuscular disease, Metabolic disease, Muscle disease, 3112 Neurosciences, 3124 Neurology and psychiatry",
author = "M. Auranen and A. Paetau and P. Piiril{\"a} and A. Pohju and T. Salmi and A. Lamminen and M. L{\"o}fberg and S. Mosegaard and Olsen, {R. K.} and T. Tyni",
year = "2017",
month = jun,
doi = "10.1016/j.nmd.2017.03.003",
language = "English",
volume = "27",
pages = "581--584",
journal = "Neuromuscular Disorders",
issn = "0960-8966",
publisher = "Elsevier Ltd. ",
number = "6",
}