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Parkinsonism & Related Disorders 2019 / 3

De-novo KMT2B mutation in a consanguineous family: 15-Year follow-up of an Afghan dystonia patient

Klein, Christine, Baumann, Hauke, Olschewski, Luisa, Hanssen, Henrike, Münchau, Alexander, Ferbert, Andreas, Brüggemann, Norbert, Lohmann, Katja
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Language:
english
Journal:
Parkinsonism & Related Disorders
DOI:
10.1016/j.parkreldis.2019.03.018
Date:
March, 2019
File:
PDF, 648 KB
english, 2019
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