GRÜNERT, Sarah, WEHRLE, Anika, VILLAVICENCIO LORINI, Pablo, LAUSCH, Ekkehart, SCHWAB, Karl Otfried, TUCCI, Sara und SPIEKERKÖTTER, Ute, 2017. Medium-chain acyl-Co A dehydrogenase deficiency associated with a novel splice mutation in the ACADM gene missed by newborn screening. Freiburg: Universität.
Elsevier - Harvard (with titles)Grünert, S., Wehrle, A., Villavicencio Lorini, P., Lausch, E., Schwab, K.O., Tucci, S., Spiekerkötter, U., 2017. Medium-chain acyl-Co A dehydrogenase deficiency associated with a novel splice mutation in the ACADM gene missed by newborn screening. Universität, Freiburg. https://doi.org/10.1186/s12881-015-0199-5
American Psychological Association 7th editionGrünert, S., Wehrle, A., Villavicencio Lorini, P., Lausch, E., Schwab, K. O., Tucci, S., & Spiekerkötter, U. (ca. 2017). Medium-chain acyl-Co A dehydrogenase deficiency associated with a novel splice mutation in the ACADM gene missed by newborn screening [Cd]. Universität. https://doi.org/10.1186/s12881-015-0199-5
Springer - Basic (author-date)Grünert S, Wehrle A, Villavicencio Lorini P, Lausch E, Schwab KO, Tucci S, Spiekerkötter U (2017) Medium-chain acyl-Co A dehydrogenase deficiency associated with a novel splice mutation in the ACADM gene missed by newborn screening. Universität, Freiburg
Juristische Zitierweise (Stüber) (Deutsch)Grünert, Sarah/ Wehrle, Anika/ Villavicencio Lorini, Pablo/ Lausch, Ekkehart/ Schwab, Karl Otfried/ Tucci, Sara/ Spiekerkötter, Ute, Medium-chain acyl-Co A dehydrogenase deficiency associated with a novel splice mutation in the ACADM gene missed by newborn screening, Freiburg 2017.