APA

Mencacci N. E., Rubio-Agusti I., Zdebik A., Asmus F., Ludtmann M. H. R., Ryten M., Plagnol V., Hauser A., Bandres-Ciga S., Bettencourt C., Forabosco P., Hughes D., Soutar M. M. P., Peall K., Morris H. R., Trabzuni D., Tekman M., Stanescu H. C., Kleta R., Carecchio M., Zorzi G., Nardocci N., Garavaglia B., Lohmann E., Weissbach A., Klein C., Hardy J., Pittman A. M., Foltynie T., Abramov A. Y., Gasser T., Bhatia K. P. & Wood N. W. (20150817). A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia. : American journal of human genetics.

Chicago

Mencacci Niccolo E, Rubio-Agusti Ignacio, Zdebik Anselm, Asmus Friedrich, Ludtmann Marthe H R, Ryten Mina, Plagnol Vincent, Hauser Ann-Kathrin, Bandres-Ciga Sara, Bettencourt Conceição, Forabosco Paola, Hughes Deborah, Soutar Marc M P, Peall Kathryn, Morris Huw R, Trabzuni Daniah, Tekman Mehmet, Stanescu Horia C, Kleta Robert, Carecchio Miryam, Zorzi Giovanna, Nardocci Nardo, Garavaglia Barbara, Lohmann Ebba, Weissbach Anne, Klein Christine, Hardy John, Pittman Alan M, Foltynie Thomas, Abramov Andrey Y, Gasser Thomas, Bhatia Kailash P and Wood Nicholas W. 20150817. A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia. : American journal of human genetics.

Harvard

Mencacci N. E., Rubio-Agusti I., Zdebik A., Asmus F., Ludtmann M. H. R., Ryten M., Plagnol V., Hauser A., Bandres-Ciga S., Bettencourt C., Forabosco P., Hughes D., Soutar M. M. P., Peall K., Morris H. R., Trabzuni D., Tekman M., Stanescu H. C., Kleta R., Carecchio M., Zorzi G., Nardocci N., Garavaglia B., Lohmann E., Weissbach A., Klein C., Hardy J., Pittman A. M., Foltynie T., Abramov A. Y., Gasser T., Bhatia K. P. and Wood N. W. (20150817). A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia. : American journal of human genetics.

MLA

Mencacci Niccolo E, Rubio-Agusti Ignacio, Zdebik Anselm, Asmus Friedrich, Ludtmann Marthe H R, Ryten Mina, Plagnol Vincent, Hauser Ann-Kathrin, Bandres-Ciga Sara, Bettencourt Conceição, Forabosco Paola, Hughes Deborah, Soutar Marc M P, Peall Kathryn, Morris Huw R, Trabzuni Daniah, Tekman Mehmet, Stanescu Horia C, Kleta Robert, Carecchio Miryam, Zorzi Giovanna, Nardocci Nardo, Garavaglia Barbara, Lohmann Ebba, Weissbach Anne, Klein Christine, Hardy John, Pittman Alan M, Foltynie Thomas, Abramov Andrey Y, Gasser Thomas, Bhatia Kailash P and Wood Nicholas W. A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia. : American journal of human genetics. 20150817.