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

Institute of Neurogenetics

Charite - Universitatsmedizin Berlin

2 Citations (Scopus)

Original language	English
Journal	Parkinsonism and Related Disorders
Volume	37
Pages (from-to)	120-122
Number of pages	3
ISSN	1353-8020
DOIs	https://doi.org/10.1016/j.parkreldis.2017.02.009
Publication status	Published - 01.04.2017

Funding

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

This output contributes to the following UN Sustainable Development Goals (SDGs)

SDG 3 Good Health and Well-being

Research Areas and Centers

Research Area: Medical Genetics

Access to Document

10.1016/j.parkreldis.2017.02.009

Cite this

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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.\}",

year = "2017",

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doi = "10.1016/j.parkreldis.2017.02.009",

language = "English",

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pages = "120--122",

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TY - JOUR

T1 - A novel de-novo mutation in the ATP1A3 gene causing rapid-onset dystonia parkinsonism

AU - Wenzel, Gregor R.

AU - Lohmann, Katja

AU - Kühn, Andrea A.

PY - 2017/4/1

Y1 - 2017/4/1

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

U2 - 10.1016/j.parkreldis.2017.02.009

DO - 10.1016/j.parkreldis.2017.02.009

M3 - Letters

C2 - 28214263

AN - SCOPUS:85012929129

SN - 1353-8020

VL - 37

SP - 120

EP - 122

JO - Parkinsonism and Related Disorders

JF - Parkinsonism and Related Disorders

ER -

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

Funding

UN SDGs

Research Areas and Centers

Access to Document

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Cite this