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John W Roberts

Showing results (21-30 of 24) with videos related to

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Archives of Neurology|November 10, 2010
SNCA variant associated with Parkinson disease and plasma alpha-synuclein levelIgnacio F Mata, Min Shi, Pinky Agarwal, et al.
Plos Genetics|August 31, 2011
Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffeeTaye H Hamza, Honglei Chen, Erin M Hill-Burns, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 2, 2012
Common variation in the LRRK2 gene is a risk factor for Parkinson's diseaseIgnacio F Mata, Harvey Checkoway, Carolyn M Hutter, et al.
Molecular Neurodegeneration|September 25, 2015
The RAB39B p.G192R mutation causes X-linked dominant Parkinson's diseaseIgnacio F Mata, Yongwoo Jang, Chun-Hyung Kim, et al.
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Showing results (21-30 of 24) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 24 results.
Archives of Neurology|November 10, 2010
SNCA variant associated with Parkinson disease and plasma alpha-synuclein levelIgnacio F Mata, Min Shi, Pinky Agarwal, et al.
Plos Genetics|August 31, 2011
Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffeeTaye H Hamza, Honglei Chen, Erin M Hill-Burns, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 2, 2012
Common variation in the LRRK2 gene is a risk factor for Parkinson's diseaseIgnacio F Mata, Harvey Checkoway, Carolyn M Hutter, et al.
Molecular Neurodegeneration|September 25, 2015
The RAB39B p.G192R mutation causes X-linked dominant Parkinson's diseaseIgnacio F Mata, Yongwoo Jang, Chun-Hyung Kim, et al.
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