APA

Muglia M., Vazza G., Patitucci A., Milani M., Pareyson D., Taroni F., Quattrone A. & Mostacciuolo M. L. (20111110). A novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern Italy. : BMJ case reports.

Chicago

Muglia Maria, Vazza Giovanni, Patitucci Alessandra, Milani Micaela, Pareyson Davide, Taroni Franco, Quattrone Aldo and Mostacciuolo Maria Luisa. 20111110. A novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern Italy. : BMJ case reports.

Harvard

Muglia M., Vazza G., Patitucci A., Milani M., Pareyson D., Taroni F., Quattrone A. and Mostacciuolo M. L. (20111110). A novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern Italy. : BMJ case reports.

MLA

Muglia Maria, Vazza Giovanni, Patitucci Alessandra, Milani Micaela, Pareyson Davide, Taroni Franco, Quattrone Aldo and Mostacciuolo Maria Luisa. A novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern Italy. : BMJ case reports. 20111110.