Genetic and phenotypic characterization of NKX6-2-related spastic ataxia and hypomyelination. [electronic resource]
By: Contributor(s):- 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
- 1468-1331
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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Genetic and phenotypic characterization of NKX6-2-related spastic ataxia and hypomyelination.
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.