APA

Farkas K., Deák B. K., Sánchez L. C., Martínez A. M. V., Corell J. J. V., Botella A. M., Benito G. M., López R. R., Vanecek T., Kazakov D. V., Kromosoeto J. N. R., van den Ouweland A. M. W., Varga J., Széll M. & Nagy N. (20161019). The CYLD p.R758X worldwide recurrent nonsense mutation detected in patients with multiple familial trichoepithelioma type 1, Brooke-Spiegler syndrome and familial cylindromatosis represents a mutational hotspot in the gene. : BMC genetics.

Chicago

Farkas Katalin, Deák Barbara Kocsis, Sánchez Laura Cubells, Martínez Ana Mercedes Victoria, Corell Juan José Vilata, Botella Alfredo Montoro, Benito Goitzane Marcaida, López Raquel Rodríguez, Vanecek Tomas, Kazakov Dmitry V, Kromosoeto Joan N R, van den Ouweland Ans M W, Varga János, Széll Márta and Nagy Nikoletta. 20161019. The CYLD p.R758X worldwide recurrent nonsense mutation detected in patients with multiple familial trichoepithelioma type 1, Brooke-Spiegler syndrome and familial cylindromatosis represents a mutational hotspot in the gene. : BMC genetics.

Harvard

Farkas K., Deák B. K., Sánchez L. C., Martínez A. M. V., Corell J. J. V., Botella A. M., Benito G. M., López R. R., Vanecek T., Kazakov D. V., Kromosoeto J. N. R., van den Ouweland A. M. W., Varga J., Széll M. and Nagy N. (20161019). The CYLD p.R758X worldwide recurrent nonsense mutation detected in patients with multiple familial trichoepithelioma type 1, Brooke-Spiegler syndrome and familial cylindromatosis represents a mutational hotspot in the gene. : BMC genetics.

MLA

Farkas Katalin, Deák Barbara Kocsis, Sánchez Laura Cubells, Martínez Ana Mercedes Victoria, Corell Juan José Vilata, Botella Alfredo Montoro, Benito Goitzane Marcaida, López Raquel Rodríguez, Vanecek Tomas, Kazakov Dmitry V, Kromosoeto Joan N R, van den Ouweland Ans M W, Varga János, Széll Márta and Nagy Nikoletta. The CYLD p.R758X worldwide recurrent nonsense mutation detected in patients with multiple familial trichoepithelioma type 1, Brooke-Spiegler syndrome and familial cylindromatosis represents a mutational hotspot in the gene. : BMC genetics. 20161019.