Single Heterozygous ATP13A2 Mutations Cause Cellular Dysfunction Associated with Parkinson's Disease

Jin Sung Park; Brianada Koentjoro; Christine Klein; Carolyn M. Sue

doi:10.1002/mds.27327

Single Heterozygous ATP13A2 Mutations Cause Cellular Dysfunction Associated with Parkinson's Disease

Jin Sung Park^*, Brianada Koentjoro, Christine Klein, Carolyn M. Sue

^*Corresponding author for this work

Institute of Neurogenetics

University of Sydney

3 Citations (Scopus)

Original language	English
Journal	Movement Disorders
Volume	33
Issue number	5
Pages (from-to)	852-854
Number of pages	3
ISSN	0885-3185
DOIs	https://doi.org/10.1002/mds.27327
Publication status	Published - 01.05.2018

Research Areas and Centers

Research Area: Medical Genetics

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10.1002/mds.27327

Cite this

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title = "Single Heterozygous ATP13A2 Mutations Cause Cellular Dysfunction Associated with Parkinson's Disease",

author = "Park, {Jin Sung} and Brianada Koentjoro and Christine Klein and Sue, {Carolyn M.}",

year = "2018",

month = may,

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journal = "Movement Disorders",

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AU - Park, Jin Sung

AU - Koentjoro, Brianada

AU - Klein, Christine

AU - Sue, Carolyn M.

PY - 2018/5/1

Y1 - 2018/5/1

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U2 - 10.1002/mds.27327

DO - 10.1002/mds.27327

M3 - Letters

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EP - 854

JO - Movement Disorders

JF - Movement Disorders

IS - 5

ER -

Single Heterozygous ATP13A2 Mutations Cause Cellular Dysfunction Associated with Parkinson's Disease

Research Areas and Centers

UN SDGs

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