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Delineating the phenotype of autosomal-recessive HPCA mutations: not only isolated dystonia!

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Bibliographische Detailangaben
Hauptverfasser: Balint, Bettina (VerfasserIn) , Charlesworth, Gavin (VerfasserIn) , Erro, Roberto (VerfasserIn) , Wood, Nicholas W. (VerfasserIn) , Bhatia, Kailash P. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 16 April 2019
In: Movement disorders
Year: 2019, Jahrgang: 34, Heft: 4, Pages: 589-592
ISSN:1531-8257
DOI:10.1002/mds.27638
Online-Zugang:Verlag, Volltext: https://doi.org/10.1002/mds.27638
Verlag, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/mds.27638
Volltext
Verfasserangaben:Bettina Balint, MD, Gavin Charlesworth, MD, PhD, Roberto Erro, MD, PhD, Nicholas W. Wood, MD, PhD and Kailash P. Bhatia, FRCP

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