APA
Brancati F., Iannicelli M., Travaglini L., Mazzotta A., Bertini E., Boltshauser E., D'Arrigo S., Emma F., Fazzi E., Gallizzi R., Gentile M., Loncarevic D., Mejaski-Bosnjak V., Pantaleoni C., Rigoli L., Salpietro C. D., Signorini S., Stringini G. R., Verloes A., Zabloka D., Dallapiccola B., Gleeson J. G. & Valente E. M. (20090410). MKS3/TMEM67 mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvement. : Human mutation.
Chicago
Brancati Francesco, Iannicelli Miriam, Travaglini Lorena, Mazzotta Annalisa, Bertini Enrico, Boltshauser Eugen, D'Arrigo Stefano, Emma Francesco, Fazzi Elisa, Gallizzi Romina, Gentile Mattia, Loncarevic Damir, Mejaski-Bosnjak Vlatka, Pantaleoni Chiara, Rigoli Luciana, Salpietro Carmelo D, Signorini Sabrina, Stringini Gilda Rita, Verloes Alain, Zabloka Dominika, Dallapiccola Bruno, Gleeson Joseph G and Valente Enza Maria. 20090410. MKS3/TMEM67 mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvement. : Human mutation.
Harvard
Brancati F., Iannicelli M., Travaglini L., Mazzotta A., Bertini E., Boltshauser E., D'Arrigo S., Emma F., Fazzi E., Gallizzi R., Gentile M., Loncarevic D., Mejaski-Bosnjak V., Pantaleoni C., Rigoli L., Salpietro C. D., Signorini S., Stringini G. R., Verloes A., Zabloka D., Dallapiccola B., Gleeson J. G. and Valente E. M. (20090410). MKS3/TMEM67 mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvement. : Human mutation.
MLA
Brancati Francesco, Iannicelli Miriam, Travaglini Lorena, Mazzotta Annalisa, Bertini Enrico, Boltshauser Eugen, D'Arrigo Stefano, Emma Francesco, Fazzi Elisa, Gallizzi Romina, Gentile Mattia, Loncarevic Damir, Mejaski-Bosnjak Vlatka, Pantaleoni Chiara, Rigoli Luciana, Salpietro Carmelo D, Signorini Sabrina, Stringini Gilda Rita, Verloes Alain, Zabloka Dominika, Dallapiccola Bruno, Gleeson Joseph G and Valente Enza Maria. MKS3/TMEM67 mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvement. : Human mutation. 20090410.