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Dysregulation of the causative genes for hereditary parkinsonism in the midbrain in Parkinson's disease.
Kim, Yun Joong; Jeon, Junbeom; Shin, Jaemoon; Kim, Nan Young; Hong, Jeong Hoon; Oh, Jae-Min; Hong, SangKyoon; Kim, Yeo Jin; Kim, Young-Eun; Kang, Suk Yun; Ma, Hyeo-Il; Lee, Unjoo; Yoon, Jeehee.
  • Kim YJ; ILSONG Institute of Life Science, Hallym University, Anyang, Korea.
  • Jeon J; Department of Neurology, Hallym University Sacred Heart hospital, Hallym University College of Medicine, Hallym University, Anyang, Korea.
  • Shin J; Hallym Institute of Translational Genomics & Bioinformatics, Hallym University Medical Center, Anyang, Korea.
  • Kim NY; Department of Computer Engineering, Hallym University, Chuncheon, Korea.
  • Hong JH; Department of Computer Engineering, Hallym University, Chuncheon, Korea.
  • Oh JM; Hallym Institute of Translational Genomics & Bioinformatics, Hallym University Medical Center, Anyang, Korea.
  • Hong S; ILSONG Institute of Life Science, Hallym University, Anyang, Korea.
  • Kim YJ; ILSONG Institute of Life Science, Hallym University, Anyang, Korea.
  • Kim YE; Hallym Institute of Translational Genomics & Bioinformatics, Hallym University Medical Center, Anyang, Korea.
  • Kang SY; Department of Neurology, Chuncheon Sacred Heart Hospital, Hallym University College of Medicine, Hallym University, Chuncheon, Korea.
  • Ma HI; Department of Neurology, Hallym University Sacred Heart hospital, Hallym University College of Medicine, Hallym University, Anyang, Korea.
  • Lee U; Department of Neurology, Hallym University Dongtan Sacred Heart Hospital, Hallym University College of Medicine, Hallym University, Dongtan, Korea.
  • Yoon J; Department of Neurology, Hallym University Sacred Heart hospital, Hallym University College of Medicine, Hallym University, Anyang, Korea.
Mov Disord ; 32(8): 1211-1220, 2017 Aug.
Article en En | MEDLINE | ID: mdl-28548297
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Sustancia Negra / Regulación de la Expresión Génica / Predisposición Genética a la Enfermedad / Trastornos Parkinsonianos / Mutación Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Año: 2017 Tipo del documento: Article
Texto completo
Imprimir
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PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Sustancia Negra / Regulación de la Expresión Génica / Predisposición Genética a la Enfermedad / Trastornos Parkinsonianos / Mutación Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Año: 2017 Tipo del documento: Article