APA
Chartier-Harlin M., Dachsel J. C., Vilariño-Güell C., Lincoln S. J., Leprêtre F., Hulihan M. M., Kachergus J., Milnerwood A. J., Tapia L., Song M., Le Rhun E., Mutez E., Larvor L., Duflot A., Vanbesien-Mailliot C., Kreisler A., Ross O. A., Nishioka K., Soto-Ortolaza A. I., Cobb S. A., Melrose H. L., Behrouz B., Keeling B. H., Bacon J. A., Hentati E., Williams L., Yanagiya A., Sonenberg N., Lockhart P. J., Zubair A. C., Uitti R. J., Aasly J. O., Krygowska-Wajs A., Opala G., Wszolek Z. K., Frigerio R., Maraganore D. M., Gosal D., Lynch T., Hutchinson M., Bentivoglio A. R., Valente E. M., Nichols W. C., Pankratz N., Foroud T., Gibson R. A., Hentati F., Dickson D. W., Destée A. & Farrer M. J. (20111122). Translation initiator EIF4G1 mutations in familial Parkinson disease. : American journal of human genetics.
Chicago
Chartier-Harlin Marie-Christine, Dachsel Justus C, Vilariño-Güell Carles, Lincoln Sarah J, Leprêtre Frédéric, Hulihan Mary M, Kachergus Jennifer, Milnerwood Austen J, Tapia Lucia, Song Mee-Sook, Le Rhun Emilie, Mutez Eugénie, Larvor Lydie, Duflot Aurélie, Vanbesien-Mailliot Christel, Kreisler Alexandre, Ross Owen A, Nishioka Kenya, Soto-Ortolaza Alexandra I, Cobb Stephanie A, Melrose Heather L, Behrouz Bahareh, Keeling Brett H, Bacon Justin A, Hentati Emna, Williams Lindsey, Yanagiya Akiko, Sonenberg Nahum, Lockhart Paul J, Zubair Abba C, Uitti Ryan J, Aasly Jan O, Krygowska-Wajs Anna, Opala Grzegorz, Wszolek Zbigniew K, Frigerio Roberta, Maraganore Demetrius M, Gosal David, Lynch Tim, Hutchinson Michael, Bentivoglio Anna Rita, Valente Enza Maria, Nichols William C, Pankratz Nathan, Foroud Tatiana, Gibson Rachel A, Hentati Faycal, Dickson Dennis W, Destée Alain and Farrer Matthew J. 20111122. Translation initiator EIF4G1 mutations in familial Parkinson disease. : American journal of human genetics.
Harvard
Chartier-Harlin M., Dachsel J. C., Vilariño-Güell C., Lincoln S. J., Leprêtre F., Hulihan M. M., Kachergus J., Milnerwood A. J., Tapia L., Song M., Le Rhun E., Mutez E., Larvor L., Duflot A., Vanbesien-Mailliot C., Kreisler A., Ross O. A., Nishioka K., Soto-Ortolaza A. I., Cobb S. A., Melrose H. L., Behrouz B., Keeling B. H., Bacon J. A., Hentati E., Williams L., Yanagiya A., Sonenberg N., Lockhart P. J., Zubair A. C., Uitti R. J., Aasly J. O., Krygowska-Wajs A., Opala G., Wszolek Z. K., Frigerio R., Maraganore D. M., Gosal D., Lynch T., Hutchinson M., Bentivoglio A. R., Valente E. M., Nichols W. C., Pankratz N., Foroud T., Gibson R. A., Hentati F., Dickson D. W., Destée A. and Farrer M. J. (20111122). Translation initiator EIF4G1 mutations in familial Parkinson disease. : American journal of human genetics.
MLA
Chartier-Harlin Marie-Christine, Dachsel Justus C, Vilariño-Güell Carles, Lincoln Sarah J, Leprêtre Frédéric, Hulihan Mary M, Kachergus Jennifer, Milnerwood Austen J, Tapia Lucia, Song Mee-Sook, Le Rhun Emilie, Mutez Eugénie, Larvor Lydie, Duflot Aurélie, Vanbesien-Mailliot Christel, Kreisler Alexandre, Ross Owen A, Nishioka Kenya, Soto-Ortolaza Alexandra I, Cobb Stephanie A, Melrose Heather L, Behrouz Bahareh, Keeling Brett H, Bacon Justin A, Hentati Emna, Williams Lindsey, Yanagiya Akiko, Sonenberg Nahum, Lockhart Paul J, Zubair Abba C, Uitti Ryan J, Aasly Jan O, Krygowska-Wajs Anna, Opala Grzegorz, Wszolek Zbigniew K, Frigerio Roberta, Maraganore Demetrius M, Gosal David, Lynch Tim, Hutchinson Michael, Bentivoglio Anna Rita, Valente Enza Maria, Nichols William C, Pankratz Nathan, Foroud Tatiana, Gibson Rachel A, Hentati Faycal, Dickson Dennis W, Destée Alain and Farrer Matthew J. Translation initiator EIF4G1 mutations in familial Parkinson disease. : American journal of human genetics. 20111122.