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

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ID: 89196
2019
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Reference Key
klein2019denovoparkinsonism Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Klein, Christine;Baumann, Hauke;Olschewski, Luisa;Hanssen, Henrike;Münchau, Alexander;Ferbert, Andreas;Brüggemann, Norbert;Lohmann, Katja;
Journal parkinsonism & related disorders
Year 2019
DOI
S1353-8020(19)30111-7
URL
Keywords
gene expression dyscalculia consanguinity de-novo mutation generalized dystonia kmt2b

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