ENDRES, Dominique, SÜSS, Patrick, MAIER, Simon, FRIEDEL, Evelyn, NICKEL, Kathrin Alexandra, ZIEGLER, Christiane, FIEBICH, Bernd L., GLOCKER, Franz Xaver, STOCK, Friedrich, EGGER, Karl, LANGE, Thomas, DACKO, Michael, VENHOFF, Nils, ERNY, Daniel, DOOSTKAM, Soroush, KOMLOSI, Katalin, DOMSCHKE, Katharina und TEBARTZ VAN ELST, Ludger, 2019. New variant of MELAS syndrome with executive dysfunction, heteroplasmic point mutation in the MT-ND4 gene (m.12015 T>C; p.Leu419 Pro) and comorbid polyglandular autoimmune syndrome type 2. Freiburg: Universität.

Endres, D., Süß, P., Maier, S., Friedel, E., Nickel, K.A., Ziegler, C., Fiebich, B.L., Glocker, F.X., Stock, F., Egger, K., Lange, T., Dacko, M., Venhoff, N., Erny, D., Doostkam, S., Komlosi, K., Domschke, K., Tebartz van Elst, L., 2019. New variant of MELAS syndrome with executive dysfunction, heteroplasmic point mutation in the MT-ND4 gene (m.12015 T>C; p.Leu419 Pro) and comorbid polyglandular autoimmune syndrome type 2. Universität, Freiburg. https://doi.org/10.3389/fimmu.2019.00412

Endres, D., Süß, P., Maier, S., Friedel, E., Nickel, K. A., Ziegler, C., Fiebich, B. L., Glocker, F. X., Stock, F., Egger, K., Lange, T., Dacko, M., Venhoff, N., Erny, D., Doostkam, S., Komlosi, K., Domschke, K., & Tebartz van Elst, L. (ca. 2019). New variant of MELAS syndrome with executive dysfunction, heteroplasmic point mutation in the MT-ND4 gene (m.12015 T>C; p.Leu419 Pro) and comorbid polyglandular autoimmune syndrome type 2 [Cd]. Universität. https://doi.org/10.3389/fimmu.2019.00412

Endres D, Süß P, Maier S, Friedel E, Nickel KA, Ziegler C, Fiebich BL, Glocker FX, Stock F, Egger K, Lange T, Dacko M, Venhoff N, Erny D, Doostkam S, Komlosi K, Domschke K, Tebartz van Elst L (2019) New variant of MELAS syndrome with executive dysfunction, heteroplasmic point mutation in the MT-ND4 gene (m.12015 T>C; p.Leu419 Pro) and comorbid polyglandular autoimmune syndrome type 2. Universität, Freiburg

Endres, Dominique/ Süß, Patrick/ Maier, Simon/ Friedel, Evelyn/ Nickel, Kathrin Alexandra/ Ziegler, Christiane/ Fiebich, Bernd L./ Glocker, Franz Xaver/ Stock, Friedrich/ Egger, Karl/ Lange, Thomas/ Dacko, Michael/ Venhoff, Nils/ Erny, Daniel/ Doostkam, Soroush/ Komlosi, Katalin/ Domschke, Katharina/ Tebartz van Elst, Ludger, New variant of MELAS syndrome with executive dysfunction, heteroplasmic point mutation in the MT-ND4 gene (m.12015 T>C; p.Leu419 Pro) and comorbid polyglandular autoimmune syndrome type 2, Freiburg 2019.