Data for: Biochemical signatures mimicking multiple carboxylase deficiency in children with mutations in MT-ATP6

Published: 9 January 2018| Version 1 | DOI: 10.17632/s2v2tw3mjk.1
Contributors:
Austin Larson, Johan Van Hove, Shanti Balasubramaniam, Bryce Heese, Lisette Estrella, George Diaz, Brett Graham, S. Lane Rutledge, Emma Glamuzina, natalie hauser, Gabriella Horvath, Amy Williamson, Clara van Karnebeek, John Christodoulou, Ronit Marom, James Weisfeld-Adams, Lindsay Burrage, Andre Mattman

Description

Concentrations of metabolites on acylcarnitine profiles for patients with mutations in MT-ATP6

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Mitochondrial Disorder

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