APA

Pasanen P., Myllykangas L., Pöyhönen M., Kiuru-Enari S., Tienari P. J., Laaksovirta H., Toppila J., Ylikallio E., Tyynismaa H. & Auranen M. (20161213). Intrafamilial clinical variability in individuals carrying the CHCHD10 mutation Gly66Val. : Acta neurologica Scandinavica.

Chicago

Pasanen P, Myllykangas L, Pöyhönen M, Kiuru-Enari S, Tienari P J, Laaksovirta H, Toppila J, Ylikallio E, Tyynismaa H and Auranen M. 20161213. Intrafamilial clinical variability in individuals carrying the CHCHD10 mutation Gly66Val. : Acta neurologica Scandinavica.

Harvard

Pasanen P., Myllykangas L., Pöyhönen M., Kiuru-Enari S., Tienari P. J., Laaksovirta H., Toppila J., Ylikallio E., Tyynismaa H. and Auranen M. (20161213). Intrafamilial clinical variability in individuals carrying the CHCHD10 mutation Gly66Val. : Acta neurologica Scandinavica.

MLA

Pasanen P, Myllykangas L, Pöyhönen M, Kiuru-Enari S, Tienari P J, Laaksovirta H, Toppila J, Ylikallio E, Tyynismaa H and Auranen M. Intrafamilial clinical variability in individuals carrying the CHCHD10 mutation Gly66Val. : Acta neurologica Scandinavica. 20161213.