Shortcast: Very long-chain acyl-CoA dehydrogenase deficiency in a Swedish cohort

from JIMD Podcasts · host Journal of Inherited Metabolic Disease

Dr David Olsson discusses the Swedish experience following the introduction of newborn screening for VLCAD deficiency. Very long-chain acyl-CoA dehydrogenase deficiency in a Swedish cohort: Clinical symptoms, newborn screening, enzyme activity, and genetics David Olsson, et al https://doi.org/10.1002/jmd2.12268

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This episode was published on May 2, 2022.

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