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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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