Murdoch Childrens Research Institute


Forschungseinrichtung

Standort der Organisation:
Melbourne, Australien


Publikationen in Kooperation mit FAU-Wissenschaftlerinnen und Wissenschaftlern


Meyer, E., Carss, K.J., Rankin, J., Nichols, J.M.E., Grozeva, D., Joseph, A.P.,... Kurian, M.A. (2016). Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia. Nature Genetics. https://dx.doi.org/10.1038/ng.3740
Head, S.I., Chan, S., Houweling, P.J., Quinlan, K.G.R., Murphy, R., Wagner, S.,... North, K.N. (2015). Altered Ca2+ Kinetics Associated with alpha-Actinin-3 Deficiency May Explain Positive Selection for ACTN3 Null Allele in Human Evolution. Plos Genetics, 11(1). https://dx.doi.org/10.1371/journal.pgen.1004862
Wagner, S., Chan, S., Murphy, R., Houweling, P., Quinlan, K., North, K.,... Friedrich, O. (2015). Speed of shortening is not altered in the alpha-actinin-3 (ACTN3) 'gene of speed' knock-out mutation in fast-twitch skeletal muscle. (pp. 66-66). Wiley-Blackwell.

Zuletzt aktualisiert 2016-15-08 um 13:24