@ARTICLE{Akhmedova1999178,
author={Akhmedova, S. and Anisimov, S. and Yakimovsky, A. and Schwartz, E.},
title={Gln→Arg 191 polymorphism of paraoxonase and Parkinson's disease},
journal={Human Heredity},
year={1999},
volume={49},
number={3},
pages={178-180},
doi={10.1159/000022868},
note={cited By 27},
url={https://www.scopus.com/inward/record.uri?eid=2-s2.0-0032587920&doi=10.1159%2f000022868&partnerID=40&md5=ffff4cd8e9c8abfe26909d68ed37a6b3},
affiliation={Lab. of Human Molecular Genetics, St. Petersburg Nucl. Phys. Institute, Russian Academy of Science, St. Petersburg, Russian Federation; Department of Normal Physiology, St. Petersburg Stt. Med. University, St. Petersburg, Russian Federation; St. Petersburg Inst. of Nucl. Phys., St. Petersburg area, Gatchina 188350, Russian Federation},
abstract={We investigated the Gln→Arg 191 polymorphism in paraoxonase (PON1) in St. Petersburg population, in three clinically differentiated groups of patients with Parkinson's disease (PD) and in the symptomatic tremor group. A new approach for Gln→Arg 191 PON1 polymorphism genotyping is suggested. No significant differences in the groups studies as compared to the controls was observed.},
author_keywords={Organophosphates;  Paraxonase;  Parkinson's disease},
correspondence_address1={Schwartz, E.; St. Petersburg Inst. Nuclear Physics, St. Petersburg area, Gatchina 188350, Russian Federation; email: schwartz@lnpi.spb.su},
issn={00015652},
coden={HUHEA},
pubmed_id={10364684},
language={English},
abbrev_source_title={Hum. Hered.},
document_type={Article},
source={Scopus},
}

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