De-novo KMT2B mutation in a consanguineous family: 15-Year follow-up of an Afghan dystonia patient.
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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;
parkinsonism & related disorders 2019 Vol. 64 pp. 337-339
254
klein2019denovoparkinsonism

Keywords

gene expression dyscalculia consanguinity de-novo mutation generalized dystonia kmt2b

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S1353-8020(19)30111-7

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