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A de novo BCL11B variant case manifesting with dystonic movement disorder regarding the article "BCL11B-related disorder in two canadian children: Expanding the clinical phenotype (Prasad et al., 2020)".

Eur J Med Genet. 2022 Nov;65(11):104635. doi: 10.1016/j.ejmg.2022.104635. Epub 2022 Oct 3. PMID: 36202297.

Authors/Editors: Harrer P, Leppmeier V, Berger A, Demund S, Winkelmann J, Berweck S, Zech M.
Publication Date: 2022

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