Description

• Title:
  Novel A18T and pA29S substitutions in α-synuclein may be associated with sporadic Parkinson's disease.
• Creator:
  Hoffman-Zacharska, Dorota;
  Koziorowski, Dariusz;
  Ross, Owen A;
  Milewski, Michał;
  Poznański, Jarosław;
  Jurek, Marta;
  Wszolek, Zbigniew K;
  Soto-Ortolaza, Alexandra;
  Sławek, Jarosław;
  Janik, Piotr;
  Jamrozik, Zygmunt;
  Potulska-Chromik, Anna;
  Jasińska-Myga, Barbara;
  Opala, Grzegorz;
  Krygowska-Wajs, Anna;
  Czyżewski, Krzysztof;
  Dickson, Dennis W;
  Bal, Jerzy;
  Friedman, Andrzej
• Description:
  Mutations in the α-synuclein-encoding gene SNCA are considered as a rare cause of Parkinson's disease (PD). Our objective was to examine the frequency of the SNCA point mutations among PD patients of Polish origin.
• Object availability:
  free access
• Date:
  2013.11
• Type:
  Article;
  PeerReviewed
• Relation: http://eprints.ibb.waw.pl/632 ;http://www.sciencedirect.com/science/article/pii/S1353802013002654 ;
  10.1016/j.parkreldis.2013.07.011
• Subject:
  R Medicine (General)
• Identifier:
  Hoffman-Zacharska, Dorota and Koziorowski, Dariusz and Ross, Owen A and Milewski, Michał and Poznański, Jarosław and Jurek, Marta and Wszolek, Zbigniew K and Soto-Ortolaza, Alexandra and Sławek, Jarosław and Janik, Piotr and Jamrozik, Zygmunt and Potulska-Chromik, Anna and Jasińska-Myga, Barbara and Opala, Grzegorz and Krygowska-Wajs, Anna and Czyżewski, Krzysztof and Dickson, Dennis W and Bal, Jerzy and Friedman, Andrzej (2013) Novel A18T and pA29S substitutions in α-synuclein may be associated with sporadic Parkinson's disease. Parkinsonism & related disorders, 19 (11). pp. 1057-60. ISSN 1873-5126
• Data provider:
  Repozytorium Instytutu Biochemii i Biofizyki Polskiej Akademii Nauk
• Can I use it?:
  seek permission
• Type:
  other