generalized dystonia

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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, Andre...
2019 parkinsonism & related disorders DOI: S1353-8020(19)30111-... 230 views

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parkinsonism & related disorders
ISSN: 1873-5126 369 views

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gene expression dyscalculia consanguinity de-novo mutation kmt2b