APA

Meyer E., Carss K. J., Rankin J., Nichols J. M. E., Grozeva D., Joseph A. P., Mencacci N. E., Papandreou A., Ng J., Barral S., Ngoh A., Ben-Pazi H., Willemsen M. A., Arkadir D., Barnicoat A., Bergman H., Bhate S., Boys A., Darin N., Foulds N., Gutowski N., Hills A., Houlden H., Hurst J. A., Israel Z., Kaminska M., Limousin P., Lumsden D., McKee S., Misra S., Mohammed S. S., Nakou V., Nicolai J., Nilsson M., Pall H., Peall K. J., Peters G. B., Prabhakar P., Reuter M. S., Rump P., Segel R., Sinnema M., Smith M., Turnpenny P., White S. M., Wieczorek D., Wiethoff S., Wilson B. T., Winter G., Wragg C., Pope S., Heales S. J. H., Morrogh D., Pittman A., Carr L. J., Perez-Dueñas B., Lin J., Reis A., Gahl W. A., Toro C., Bhatia K. P., Wood N. W., Kamsteeg E., Chong W. K., Gissen P., Topf M., Dale R. C., Chubb J. R., Raymond F. L. & Kurian M. A. (052017). Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia. : Nature genetics.

Chicago

Meyer Esther, Carss Keren J, Rankin Julia, Nichols John M E, Grozeva Detelina, Joseph Agnel P, Mencacci Niccolo E, Papandreou Apostolos, Ng Joanne, Barral Serena, Ngoh Adeline, Ben-Pazi Hilla, Willemsen Michel A, Arkadir David, Barnicoat Angela, Bergman Hagai, Bhate Sanjay, Boys Amber, Darin Niklas, Foulds Nicola, Gutowski Nicholas, Hills Alison, Houlden Henry, Hurst Jane A, Israel Zvi, Kaminska Margaret, Limousin Patricia, Lumsden Daniel, McKee Shane, Misra Shibalik, Mohammed Shekeeb S, Nakou Vasiliki, Nicolai Joost, Nilsson Magnus, Pall Hardev, Peall Kathryn J, Peters Gregory B, Prabhakar Prab, Reuter Miriam S, Rump Patrick, Segel Reeval, Sinnema Margje, Smith Martin, Turnpenny Peter, White Susan M, Wieczorek Dagmar, Wiethoff Sarah, Wilson Brian T, Winter Gidon, Wragg Christopher, Pope Simon, Heales Simon J H, Morrogh Deborah, Pittman Alan, Carr Lucinda J, Perez-Dueñas Belen, Lin Jean-Pierre, Reis Andre, Gahl William A, Toro Camilo, Bhatia Kailash P, Wood Nicholas W, Kamsteeg Erik-Jan, Chong Wui K, Gissen Paul, Topf Maya, Dale Russell C, Chubb Jonathan R, Raymond F Lucy and Kurian Manju A. 052017. Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia. : Nature genetics.

Harvard

Meyer E., Carss K. J., Rankin J., Nichols J. M. E., Grozeva D., Joseph A. P., Mencacci N. E., Papandreou A., Ng J., Barral S., Ngoh A., Ben-Pazi H., Willemsen M. A., Arkadir D., Barnicoat A., Bergman H., Bhate S., Boys A., Darin N., Foulds N., Gutowski N., Hills A., Houlden H., Hurst J. A., Israel Z., Kaminska M., Limousin P., Lumsden D., McKee S., Misra S., Mohammed S. S., Nakou V., Nicolai J., Nilsson M., Pall H., Peall K. J., Peters G. B., Prabhakar P., Reuter M. S., Rump P., Segel R., Sinnema M., Smith M., Turnpenny P., White S. M., Wieczorek D., Wiethoff S., Wilson B. T., Winter G., Wragg C., Pope S., Heales S. J. H., Morrogh D., Pittman A., Carr L. J., Perez-Dueñas B., Lin J., Reis A., Gahl W. A., Toro C., Bhatia K. P., Wood N. W., Kamsteeg E., Chong W. K., Gissen P., Topf M., Dale R. C., Chubb J. R., Raymond F. L. and Kurian M. A. (052017). Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia. : Nature genetics.

MLA

Meyer Esther, Carss Keren J, Rankin Julia, Nichols John M E, Grozeva Detelina, Joseph Agnel P, Mencacci Niccolo E, Papandreou Apostolos, Ng Joanne, Barral Serena, Ngoh Adeline, Ben-Pazi Hilla, Willemsen Michel A, Arkadir David, Barnicoat Angela, Bergman Hagai, Bhate Sanjay, Boys Amber, Darin Niklas, Foulds Nicola, Gutowski Nicholas, Hills Alison, Houlden Henry, Hurst Jane A, Israel Zvi, Kaminska Margaret, Limousin Patricia, Lumsden Daniel, McKee Shane, Misra Shibalik, Mohammed Shekeeb S, Nakou Vasiliki, Nicolai Joost, Nilsson Magnus, Pall Hardev, Peall Kathryn J, Peters Gregory B, Prabhakar Prab, Reuter Miriam S, Rump Patrick, Segel Reeval, Sinnema Margje, Smith Martin, Turnpenny Peter, White Susan M, Wieczorek Dagmar, Wiethoff Sarah, Wilson Brian T, Winter Gidon, Wragg Christopher, Pope Simon, Heales Simon J H, Morrogh Deborah, Pittman Alan, Carr Lucinda J, Perez-Dueñas Belen, Lin Jean-Pierre, Reis Andre, Gahl William A, Toro Camilo, Bhatia Kailash P, Wood Nicholas W, Kamsteeg Erik-Jan, Chong Wui K, Gissen Paul, Topf Maya, Dale Russell C, Chubb Jonathan R, Raymond F Lucy and Kurian Manju A. Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia. : Nature genetics. 052017.