| 1 | CACNA1B, DYT23, DYT26, DYT4, KCTD17, TUBB4A
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| Novel Dystonia Genes: Clues on Disease Mechanisms and the Complexities of High-Throughput Sequencing.
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| Domingo A, Erro R, Lohmann K.
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| Mov Disord 31(4):471-7. doi: 10.1002/mds.26600. Review.
2016
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| 2 | CACNA1B, DYT23
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| CACNA1B mutation is linked to unique myoclonus-dystonia syndrome.
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| Groen JL, Andrade A, Ritz K, Jalalzadeh H, Haagmans M, Bradley TE, Jongejan A, Verbeek DS, Nürnberg P, Denome S, Hennekam RC, Lipscombe D, Baas F, Tijssen MA.
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| Hum Mol Genet 24(4):987-93. doi: 10.1093/hmg/ddu513.
2015
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| 3 | ANO3, CACNA1B, DYT23, DYT24, DYT25, GNAL
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| Dystonia: an update on phenomenology, classification, pathogenesis and treatment.
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| Balint B, Bhatia KP.
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| Curr Opin Neurol 27(4):468-76. doi: 10.1097/WCO.0000000000000114. Review.
2014
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| 4 | DYT23
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| A new familial syndrome with dystonia and lower limb action myoclonus.
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| Groen J, van Rootselaar AF, van der Salm SM, Bloem BR, Tijssen M.
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| Mov Disord 26(5):896-900. doi: 10.1002/mds.23557.
2011
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