APA
Chelban V., Alsagob M., Kloth K., Chirita-Emandi A., Vandrovcova J., Maroofian R., Davagnanam I., Bakhtiari S., AlSayed M. D., Rahbeeni Z., AlZaidan H., Malintan N. T., Johannsen J., Efthymiou S., Ghayoor Karimiani E., Mankad K., Al-Shahrani S. A., Beiraghi Toosi M., AlShammari M., Groppa S., Haridy N. A., AlQuait L., Qari A., Huma R., Salih M. A., Almass R., Almutairi F. B., Hamad M. H., Alorainy I. A., Ramzan K., Imtiaz F., Puiu M., Kruer M. C., Bierhals T., Wood N. W., Colak D., Houlden H. & Kaya N. (20210624). Genetic and phenotypic characterization of NKX6-2-related spastic ataxia and hypomyelination. : European journal of neurology.
Chicago
Chelban V, Alsagob M, Kloth K, Chirita-Emandi A, Vandrovcova J, Maroofian R, Davagnanam I, Bakhtiari S, AlSayed M D, Rahbeeni Z, AlZaidan H, Malintan N T, Johannsen J, Efthymiou S, Ghayoor Karimiani E, Mankad K, Al-Shahrani S A, Beiraghi Toosi M, AlShammari M, Groppa S, Haridy N A, AlQuait L, Qari A, Huma R, Salih M A, Almass R, Almutairi F B, Hamad M H, Alorainy I A, Ramzan K, Imtiaz F, Puiu M, Kruer M C, Bierhals T, Wood N W, Colak D, Houlden H and Kaya N. 20210624. Genetic and phenotypic characterization of NKX6-2-related spastic ataxia and hypomyelination. : European journal of neurology.
Harvard
Chelban V., Alsagob M., Kloth K., Chirita-Emandi A., Vandrovcova J., Maroofian R., Davagnanam I., Bakhtiari S., AlSayed M. D., Rahbeeni Z., AlZaidan H., Malintan N. T., Johannsen J., Efthymiou S., Ghayoor Karimiani E., Mankad K., Al-Shahrani S. A., Beiraghi Toosi M., AlShammari M., Groppa S., Haridy N. A., AlQuait L., Qari A., Huma R., Salih M. A., Almass R., Almutairi F. B., Hamad M. H., Alorainy I. A., Ramzan K., Imtiaz F., Puiu M., Kruer M. C., Bierhals T., Wood N. W., Colak D., Houlden H. and Kaya N. (20210624). Genetic and phenotypic characterization of NKX6-2-related spastic ataxia and hypomyelination. : European journal of neurology.
MLA
Chelban V, Alsagob M, Kloth K, Chirita-Emandi A, Vandrovcova J, Maroofian R, Davagnanam I, Bakhtiari S, AlSayed M D, Rahbeeni Z, AlZaidan H, Malintan N T, Johannsen J, Efthymiou S, Ghayoor Karimiani E, Mankad K, Al-Shahrani S A, Beiraghi Toosi M, AlShammari M, Groppa S, Haridy N A, AlQuait L, Qari A, Huma R, Salih M A, Almass R, Almutairi F B, Hamad M H, Alorainy I A, Ramzan K, Imtiaz F, Puiu M, Kruer M C, Bierhals T, Wood N W, Colak D, Houlden H and Kaya N. Genetic and phenotypic characterization of NKX6-2-related spastic ataxia and hypomyelination. : European journal of neurology. 20210624.