Brockmann, S.J., Freischmidt, A., Oeckl, P., Müller, K., Ponna, S.K., Helferich, A.M., Paone, C., Reinders, J., Kojer, K., Orth, M., Jokela, M., Auranen, M., Udd, B., Hermann, A., Danzer, K.M., Lichtner, P., Walther, P., Ludolph, A.C., Andersen, P.M., Otto, M., Kursula, P., Just, S., Weishaupt, J.H. (2018) CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiency. Human molecular genetics. 27(4):706-715

Brockmann, S.J., Freischmidt, A., Oeckl, P., Müller, K., Ponna, S.K., Helferich, A.M., Paone, C., Reinders, J., Kojer, K., Orth, M., Jokela, M., Auranen, M., Udd, B., Hermann, A., Danzer, K.M., Lichtner, P., Walther, P., Ludolph, A.C., Andersen, P.M., Otto, M., Kursula, P., Just, S., Weishaupt, J.H. (2018) CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiency. Human molecular genetics. 27(4):706-715