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HARVARD Citation
Klein, C. et al. (2019). De-novo KMT2B mutation in a consanguineous family: 15-Year follow-up of an Afghan dystonia patient. Parkinsonism & related disorders. pp. 337-339. [Online].
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Klein, C. et al. (2019). De-novo KMT2B mutation in a consanguineous family: 15-Year follow-up of an Afghan dystonia patient. Parkinsonism & related disorders. pp. 337-339. [Online].