Juvenile onset Parkinsonism with “pure nigral” degeneration and POLG1 mutation

Shyamal H. Mehta; Dennis W. Dickson; John C. Morgan; Andrew B. Singleton; Elisa Majounie; Kapil D. Sethi

doi:10.1016/j.parkreldis.2016.06.013

Juvenile onset Parkinsonism with “pure nigral” degeneration and POLG1 mutation

Shyamal H. Mehta, Dennis W. Dickson, John C. Morgan, Andrew B. Singleton, Elisa Majounie, Kapil D. Sethi

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

Original language	English (US)
Pages (from-to)	83-85
Number of pages	3
Journal	Parkinsonism and Related Disorders
Volume	30
DOIs	https://doi.org/10.1016/j.parkreldis.2016.06.013
State	Published - Sep 1 2016

ASJC Scopus subject areas

Neurology
Geriatrics and Gerontology
Clinical Neurology

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10.1016/j.parkreldis.2016.06.013

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@article{a0092a2d6bb14d51b567161b535758e6,

title = "Juvenile onset Parkinsonism with “pure nigral” degeneration and POLG1 mutation",

author = "Mehta, \{Shyamal H.\} and Dickson, \{Dennis W.\} and Morgan, \{John C.\} and Singleton, \{Andrew B.\} and Elisa Majounie and Sethi, \{Kapil D.\}",

note = "Funding Information: Dr. Sethi reports personal fees from Merz Pharmaceuticals, personal fees from Teva, personal fees from Impax Labs, personal fees from Veloxis, personal fees from Lundbeck, personal fees from Synosia, grants from NIH, grants from NPF, grants from Kyowa, grants from Acadia, grants from Abbvie, outside the submitted work. Funding Information: We would like to thank Ava Mahloogi for the gene sequencing at the Laboratory of Neurogenetics, National Institute on Aging, Bethesda, MD, 20892, USA. Supported by P50-NS72187 (DWD) and the Mangurian Foundation (DWD).",

year = "2016",

month = sep,

day = "1",

doi = "10.1016/j.parkreldis.2016.06.013",

language = "English (US)",

volume = "30",

pages = "83--85",

journal = "Parkinsonism and Related Disorders",

issn = "1353-8020",

publisher = "Elsevier Ltd",

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TY - JOUR

T1 - Juvenile onset Parkinsonism with “pure nigral” degeneration and POLG1 mutation

AU - Mehta, Shyamal H.

AU - Dickson, Dennis W.

AU - Morgan, John C.

AU - Singleton, Andrew B.

AU - Majounie, Elisa

AU - Sethi, Kapil D.

N1 - Funding Information: Dr. Sethi reports personal fees from Merz Pharmaceuticals, personal fees from Teva, personal fees from Impax Labs, personal fees from Veloxis, personal fees from Lundbeck, personal fees from Synosia, grants from NIH, grants from NPF, grants from Kyowa, grants from Acadia, grants from Abbvie, outside the submitted work. Funding Information: We would like to thank Ava Mahloogi for the gene sequencing at the Laboratory of Neurogenetics, National Institute on Aging, Bethesda, MD, 20892, USA. Supported by P50-NS72187 (DWD) and the Mangurian Foundation (DWD).

PY - 2016/9/1

Y1 - 2016/9/1

UR - https://www.scopus.com/pages/publications/84977537971

UR - https://www.scopus.com/inward/citedby.url?scp=84977537971&partnerID=8YFLogxK

U2 - 10.1016/j.parkreldis.2016.06.013

DO - 10.1016/j.parkreldis.2016.06.013

M3 - Letter

C2 - 27349602

AN - SCOPUS:84977537971

SN - 1353-8020

VL - 30

SP - 83

EP - 85

JO - Parkinsonism and Related Disorders

JF - Parkinsonism and Related Disorders

ER -

Juvenile onset Parkinsonism with “pure nigral” degeneration and POLG1 mutation

ASJC Scopus subject areas

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