APA
Logan C. V., Szabadkai G., Sharpe J. A., Parry D. A., Torelli S., Childs A., 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. (20140325). Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling. : Nature genetics.
Chicago
Logan Clare V, Szabadkai György, Sharpe Jenny A, Parry David A, Torelli Silvia, Childs Anne-Marie, Kriek Marjolein, Phadke Rahul, Johnson Colin A, Roberts Nicola Y, Bonthron David T, Pysden Karen A, Whyte Tamieka, Munteanu Iulia, Foley A Reghan, Wheway Gabrielle, Szymanska Katarzyna, Natarajan Subaashini, Abdelhamed Zakia A, Morgan Joanne E, Roper Helen, Santen Gijs W E, Niks Erik H, van der Pol W Ludo, Lindhout Dick, Raffaello Anna, De Stefani Diego, den Dunnen Johan T, Sun Yu, Ginjaar Ieke, Sewry Caroline A, Hurles Matthew, Rizzuto Rosario, Duchen Michael R, Muntoni Francesco and Sheridan Eamonn. 20140325. Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling. : Nature genetics.
Harvard
Logan C. V., Szabadkai G., Sharpe J. A., Parry D. A., Torelli S., Childs A., 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. and Sheridan E. (20140325). Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling. : Nature genetics.
MLA
Logan Clare V, Szabadkai György, Sharpe Jenny A, Parry David A, Torelli Silvia, Childs Anne-Marie, Kriek Marjolein, Phadke Rahul, Johnson Colin A, Roberts Nicola Y, Bonthron David T, Pysden Karen A, Whyte Tamieka, Munteanu Iulia, Foley A Reghan, Wheway Gabrielle, Szymanska Katarzyna, Natarajan Subaashini, Abdelhamed Zakia A, Morgan Joanne E, Roper Helen, Santen Gijs W E, Niks Erik H, van der Pol W Ludo, Lindhout Dick, Raffaello Anna, De Stefani Diego, den Dunnen Johan T, Sun Yu, Ginjaar Ieke, Sewry Caroline A, Hurles Matthew, Rizzuto Rosario, Duchen Michael R, Muntoni Francesco and Sheridan Eamonn. Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling. : Nature genetics. 20140325.