Mitochondrial DNA Haplogroups and Three Independent Polymorphisms have no Association with the Risk of Parkinson's Disease in East Indian Population.

Saha, Tania; Roy, Somrita; Chakraborty, Rajashree; Biswas, Arindam; Das, Shyamal K; Ray, Kunal; Ray, Jharna; Sengupta, Mainak

Saha, Tania; Roy, Somrita; Chakraborty, Rajashree; Biswas, Arindam; Das, Shyamal K; Ray, Kunal; Ray, Jharna; Sengupta, Mainak.

Afiliação

Saha T; Department of Genetics, University of Calcutta, Kolkata, West Bengal, India.
Roy S; Department of Genetics, University of Calcutta, Kolkata, West Bengal, India.
Chakraborty R; Department of Genetics, University of Calcutta, Kolkata, West Bengal, India.
Biswas A; S. N. Pradhan Centre for Neurosciences, University of Calcutta, Kolkata, West Bengal, India.
Das SK; Movement Disorders Clinic, Bangur Institute of Neurosciences, Kolkata, West Bengal, India.
Ray K; School of Biological Sciences, RKMVERI, Narendrapur, West Bengal, India.
Ray J; S. N. Pradhan Centre for Neurosciences, University of Calcutta, Kolkata, West Bengal, India.
Sengupta M; Department of Genetics, University of Calcutta, Kolkata, West Bengal, India.

Neurol India ; 69(2): 461-465, 2021.

Article em En | MEDLINE | ID: mdl-33904476

Assuntos

DNA Mitocondrial; Doença de Parkinson; Povo Asiático; DNA Mitocondrial/genética; Genótipo; Haplótipos; Humanos; Índia; Doença de Parkinson/genética; Polimorfismo de Nucleotídeo Único/genética

Palavras-chave

Genetic Association; Haplogroups; Mitochondrial DNA; Parkinson's disease; SNP

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / DNA Mitocondrial Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Humans País/Região como assunto: Asia Idioma: En Revista: Neurol India Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Índia

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