TY  - JOUR
AU  - Vulinovic, Franca
AU  - Schaake, Susen
AU  - Domingo, Aloysius
AU  - Kumar, Kishore Raj
AU  - Defazio, Giovanni
AU  - Mir, Pablo
AU  - Simonyan, Kristina
AU  - Ozelius, Laurie J
AU  - Brüggemann, Norbert
AU  - Chung, Sun Ju
AU  - Rakovic, Aleksandar
AU  - Lohmann, Katja
AU  - Klein, Christine
PY  - 2017
DO  - 10.1016/j.parkreldis.2017.06.001
UR  - http://hdl.handle.net/10668/11350
T2  - Parkinsonism & related disorders
AB  - Mutations in TUBB4A have been identified to cause a wide phenotypic spectrum ranging from hereditary generalized dystonia with whispering dysphonia (DYT4) to the leukodystrophy hypomyelination syndrome with atrophy of the basal ganglia and cerebellum...
LA  - en
KW  - Dystonia
KW  - H-ABC
KW  - Leukodystrophy
KW  - TUBB4A
KW  - Adult
KW  - Age of Onset
KW  - Aged
KW  - DNA Mutational Analysis
KW  - Dystonia
KW  - Female
KW  - Genetic Association Studies
KW  - Humans
KW  - International Cooperation
KW  - Male
KW  - Middle Aged
KW  - Mutation
KW  - Tubulin
TI  - Screening study of TUBB4A in isolated dystonia.
TY  - research article
VL  - 41
ER  -