Novel ATP1A3 mutation in a sporadic RDP patient with minimal benefit from deep brain stimulation

C. Kamm; W. Fogel; T. Wächter; K. Schweitzer; D. Berg; R. Kruger; D. Freudenstein; T. Gasser

doi:10.1212/01.wnl.0000310431.41036.e0

Novel ATP1A3 mutation in a sporadic RDP patient with minimal benefit from deep brain stimulation

C. Kamm, W. Fogel, T. Wächter, K. Schweitzer, D. Berg, R. Kruger, D. Freudenstein, T. Gasser^*

^*Corresponding author for this work

Research output: Contribution to journal › Article › Research › peer-review

48 Citations (Scopus)

Original language	English
Pages (from-to)	1501-1503
Number of pages	3
Journal	Neurology
Volume	70
Issue number	16 PART 2
DOIs	https://doi.org/10.1212/01.wnl.0000310431.41036.e0
Publication status	Published - Apr 2008
Externally published	Yes

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@article{b7c5d0d2f795490f80606439f7319a9f,

title = "Novel ATP1A3 mutation in a sporadic RDP patient with minimal benefit from deep brain stimulation",

author = "C. Kamm and W. Fogel and T. W{\"a}chter and K. Schweitzer and D. Berg and R. Kruger and D. Freudenstein and T. Gasser",

note = "Funding Information: Supported in part by the German Network for Hereditary Movement Disorders (GeNeMove, 01 GM 0304), financed by the German Ministry for Research and Education. ",

year = "2008",

month = apr,

doi = "10.1212/01.wnl.0000310431.41036.e0",

language = "English",

volume = "70",

pages = "1501--1503",

journal = "Neurology",

issn = "0028-3878",

publisher = "Lippincott Williams and Wilkins",

number = "16 PART 2",

}

TY - JOUR

T1 - Novel ATP1A3 mutation in a sporadic RDP patient with minimal benefit from deep brain stimulation

AU - Kamm, C.

AU - Fogel, W.

AU - Wächter, T.

AU - Schweitzer, K.

AU - Berg, D.

AU - Kruger, R.

AU - Freudenstein, D.

AU - Gasser, T.

N1 - Funding Information: Supported in part by the German Network for Hereditary Movement Disorders (GeNeMove, 01 GM 0304), financed by the German Ministry for Research and Education.

PY - 2008/4

Y1 - 2008/4

UR - https://www.scopus.com/pages/publications/42049101626

U2 - 10.1212/01.wnl.0000310431.41036.e0

DO - 10.1212/01.wnl.0000310431.41036.e0

M3 - Article

AN - SCOPUS:42049101626

SN - 0028-3878

VL - 70

SP - 1501

EP - 1503

JO - Neurology

JF - Neurology

IS - 16 PART 2

ER -

Novel ATP1A3 mutation in a sporadic RDP patient with minimal benefit from deep brain stimulation

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