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Understanding the role of genetic variability in LRRK2 in Indian population.
Kishore, Asha; Ashok Kumar Sreelatha, Ashwin; Sturm, Marc; von-Zweydorf, Felix; Pihlstrøm, Lasse; Raimondi, Francesco; Russell, Rob; Lichtner, Peter; Banerjee, Moinak; Krishnan, Syam; Rajan, Roopa; Puthenveedu, Divya Kalikavil; Chung, Sun Ju; Bauer, Peter; Riess, Olaf; Gloeckner, Christian Johannes; Kruger, Rejko; Gasser, Thomas; Sharma, Manu.
Afiliação
  • Kishore A; Sree Chitra Tirunal Institute for Medical Science and Technology, Kerala, India.
  • Ashok Kumar Sreelatha A; Centre for Genetic Epidemiology, Institute for Clinical Epidemiology and Applied Biometry, University of Tübingen, Tübingen, Germany.
  • Sturm M; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
  • von-Zweydorf F; German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
  • Pihlstrøm L; Institute for Ophthalmic Research, Center for Ophthalmology, University of Tübingen, Tübingen, Germany.
  • Raimondi F; Department of Neurology, Oslo University Hospital, Oslo, Norway.
  • Russell R; Cell Networks, University of Heidelberg, Heidelberg, Germany.
  • Lichtner P; Cell Networks, University of Heidelberg, Heidelberg, Germany.
  • Banerjee M; Institute of Human Genetics, Helmholtz Zentrum München, Neuherberg, Germany.
  • Krishnan S; Rajiv Gandhi Centre for Biotechnology, Kerala, India.
  • Rajan R; Sree Chitra Tirunal Institute for Medical Science and Technology, Kerala, India.
  • Puthenveedu DK; Sree Chitra Tirunal Institute for Medical Science and Technology, Kerala, India.
  • Chung SJ; All India Institute for Medical Sciences, New Delhi, India.
  • Gloeckner CJ; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
  • Kruger R; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
  • Gasser T; German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
  • Sharma M; Institute for Ophthalmic Research, Center for Ophthalmology, University of Tübingen, Tübingen, Germany.
Mov Disord ; 34(4): 496-505, 2019 04.
Article em En | MEDLINE | ID: mdl-30485545
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Variação Genética / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Serina-Treonina Proteína Quinase-2 com Repetições Ricas em Leucina Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: Mov Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Índia
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Variação Genética / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Serina-Treonina Proteína Quinase-2 com Repetições Ricas em Leucina Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: Mov Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Índia