PuSH - Publication Server of Helmholtz Zentrum München: 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).".

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Harrer, P. ; Leppmeier, V.* ; Berger, A.* ; Demund, S.* ; Winkelmann, J. ; Berweck, S.* ; Zech, M.

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. 65:104635 (2022)

Open Access Green as soon as Postprint is submitted to ZB.

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Publication type Article: Journal article

Document type Scientific Article

ISSN (print) / ISBN 1769-7212

e-ISSN 1729-7212

Quellenangaben Volume: 65, Issue: 11, Article Number: 104635

Publisher Elsevier

Reviewing status Peer reviewed

Institute(s) Institute of Neurogenomics (ING)