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LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews.
Author(s):
Christine Klein
,
Shanda Hunt
,
Neil Risch
,
Erin Ohmann
,
Brian Henick
,
Richard Lipton
,
Amanda Deligtisch
,
Laurie J Ozelius
,
Rachel Saunders
,
Susan Hailpern
,
Michele Tagliati
,
J Valencia
,
S Bressman
,
G. Senthil
Publication date:
2006-01-26
Journal:
The New England journal of medicine
Keywords:
Europe
,
ethnology
,
Heterozygote
,
Homozygote
,
Humans
,
Jews
,
genetics
,
Mutation
,
New York City
,
Parkinson Disease
,
Protein-Serine-Threonine Kinases
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PubMed
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There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.
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iGEM
Author and article information
Journal
PubMed ID::
16436782
DOI::
10.1056/NEJMc055509
ScienceOpen disciplines:
Chemistry
Keywords:
Europe
,
ethnology
,
Heterozygote
,
Homozygote
,
Humans
,
Jews
,
genetics
,
Mutation
,
New York City
,
Parkinson Disease
,
Protein-Serine-Threonine Kinases
Data availability:
ScienceOpen disciplines:
Chemistry
Keywords:
Europe
,
ethnology
,
Heterozygote
,
Homozygote
,
Humans
,
Jews
,
genetics
,
Mutation
,
New York City
,
Parkinson Disease
,
Protein-Serine-Threonine Kinases
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