Murdoch Childrens Research Institute


Standort der Organisation:
Melbourne, Australien

Publikationen in Kooperation mit FAU-Wissenschaftern

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.
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).
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