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).”

Philip Harrer, Verena Leppmeier, Andrea Berger, Simone Demund, Juliane Winkelmann, Steffen Berweck, Michael Zech

Research output: Contribution to journalLetterpeer-review

4 Scopus citations
Original languageEnglish
Article number104635
JournalEuropean Journal of Medical Genetics
Volume65
Issue number11
DOIs
StatePublished - Nov 2022

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