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

1 Citation (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

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Research Area: Medical Genetics

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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.}",

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

language = "English",

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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 - http://www.scopus.com/inward/record.url?scp=85012929129&partnerID=8YFLogxK

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

Research Areas and Centers

UN SDGs

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