A novel de-novo mutation in the ATP1A3 gene causing rapid-onset dystonia parkinsonism

Gregor R. Wenzel; Katja Lohmann; Andrea A. Kühn

doi:10.1016/j.parkreldis.2017.02.009

A novel de-novo mutation in the ATP1A3 gene causing rapid-onset dystonia parkinsonism

Gregor R. Wenzel, Katja Lohmann, Andrea A. Kühn

Institut für Neurogenetik

Charite - Universitatsmedizin Berlin

2 Zitate (Scopus)

Originalsprache	Englisch
Zeitschrift	Parkinsonism and Related Disorders
Jahrgang	37
Seiten (von - bis)	120-122
Seitenumfang	3
ISSN	1353-8020
DOIs	https://doi.org/10.1016/j.parkreldis.2017.02.009
Publikationsstatus	Veröffentlicht - 01.04.2017

Fördermittel

Andrea Kühn received honoraria for consultancies and travel grants from Boston Scientific and Medtronic . AAK receives funding from the German Research Foundation (grant KFO247 ) grant and the German Ministry of Education and Research (BMBF, DYSTRACT consortium, grant-no. 01GM1514D ). Katja Lohmann receives funding from the German Research Foundation and the German Ministry of Education and Research (BMBF, DYSTRACT consortium, grant-no. 01GM1514B ).

UN SDGs

Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

SDG 3 – Gesundheit und Wohlergehen

Strategische Forschungsbereiche und Zentren

Querschnittsbereich: Medizinische Genetik

Dokumente

10.1016/j.parkreldis.2017.02.009

Weitere Links

Link to publication in Scopus

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title = "A novel de-novo mutation in the ATP1A3 gene causing rapid-onset dystonia parkinsonism",

author = "Wenzel, \{Gregor R.\} and Katja Lohmann and K{\"u}hn, \{Andrea A.\}",

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AU - Wenzel, Gregor R.

AU - Lohmann, Katja

AU - Kühn, Andrea A.

PY - 2017/4/1

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UR - https://www.scopus.com/pages/publications/85012929129

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DO - 10.1016/j.parkreldis.2017.02.009

M3 - Letters

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JO - Parkinsonism and Related Disorders

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