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A Possible Modifying Effect of the G2019S Mutation in the LRRK2 Gene on GBA Parkinson's Disease.
Omer, Nurit; Giladi, Nir; Gurevich, Tanya; Bar-Shira, Anat; Gana-Weisz, Mali; Goldstein, Orly; Kestenbaum, Meir; Cedarbaum, Jesse M; Orr-Urtreger, Avi; Mirelman, Anat; Thaler, Avner.
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  • Omer N; Movement Disorders Unit, Neurological Institute, Tel-Aviv Medical Center, Tel-Aviv, Israel.
  • Giladi N; Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
  • Gurevich T; Movement Disorders Unit, Neurological Institute, Tel-Aviv Medical Center, Tel-Aviv, Israel.
  • Bar-Shira A; Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
  • Gana-Weisz M; Sagol School of Neuroscience, Tel-Aviv University, Tel-Aviv, Israel.
  • Goldstein O; Movement Disorders Unit, Neurological Institute, Tel-Aviv Medical Center, Tel-Aviv, Israel.
  • Kestenbaum M; Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
  • Cedarbaum JM; Sagol School of Neuroscience, Tel-Aviv University, Tel-Aviv, Israel.
  • Orr-Urtreger A; Genetic Institute, Tel-Aviv Medical Center, Tel-Aviv, Israel.
  • Mirelman A; Genomic Research Laboratory for Neurodegeneration, Tel-Aviv Medical Center, Tel-Aviv, Israel.
  • Thaler A; Genomic Research Laboratory for Neurodegeneration, Tel-Aviv Medical Center, Tel-Aviv, Israel.
Mov Disord ; 35(7): 1249-1253, 2020 07.
Article en En | MEDLINE | ID: mdl-32353202
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Enfermedad de Parkinson Idioma: En Revista: Mov Disord Asunto de la revista: NEUROLOGIA Año: 2020 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Enfermedad de Parkinson Idioma: En Revista: Mov Disord Asunto de la revista: NEUROLOGIA Año: 2020 Tipo del documento: Article