P24 Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signalling

Autor:	Sharpe, J.A., Logan, C.V., Szabadkai, G., Parry, D.A., Torelli, S., Childs, A.-M., Kriek, M., Phadke, R., Johnson, C.A., Roberts, N.Y., Bonthron, D.T., Pysden, K.A., Whyte, T., Munteanu, I., Foley, A.R., Wheway, G., Szymanska, K., Natarajan, S., Abdelhamed, Z.A., Morgan, J.E., Roper, H., Santen, G.W.E., Niks, E.H., van der Pol, W.L., Lindhout, D., Raffaello, A., De Stefani, D., den Dunnen, J.T., Sun, Y., Ginjaar, I., Sewry, C.A., Hurles, M., Rizzuto, R., Duchen, M.R., Muntoni, F., Sheridan, E.
Zdroj:	In Neuromuscular Disorders March 2014 24 Supplement 1:S13-S13
Databáze:	ScienceDirect
Externí odkaz:	Zobrazit plný text záznamu Full Text from ScienceDirect