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).".

Title:: 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).".
Document type:: Case Reports; Letter; Comment
Author(s):: Harrer, Philip; Leppmeier, Verena; Berger, Andrea; Demund, Simone; Winkelmann, Juliane; Berweck, Steffen; Zech, Michael
Journal title abbreviation:: Eur J Med Genet
Year:: 2022
Journal volume:: 65
Journal issue:: 11
Fulltext / DOI:: doi:10.1016/j.ejmg.2022.104635
Pubmed ID:: http://view.ncbi.nlm.nih.gov/pubmed/36202297
Print-ISSN:: 1769-7212
TUM Institution:: Institut für Humangenetik; Lehrstuhl für Neurogenetik (N.N.)
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