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Clinico-pathological and Molecular Spectrum of Mitochondrial Polymerase γ Mutations in a Cohort from India.
Deepha, Sekar; Govindaraj, Periyasamy; Sankaran, Bindu Parayil; Chiplunkar, Shwetha; Kashinkunti, Chetan; Nunia, Vandana; Nagappa, Madhu; Sinha, Sanjib; Khanna, Tripti; Thangaraj, Kumarasamy; Taly, Arun B; Gayathri, Narayanappa.
Afiliação
  • Deepha S; Department of Neuropathology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India.
  • Govindaraj P; Neuromuscular Laboratory, Neurobiology Research Centre (NRC), National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India.
  • Sankaran BP; Department of Neuropathology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India.
  • Chiplunkar S; Neuromuscular Laboratory, Neurobiology Research Centre (NRC), National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India.
  • Kashinkunti C; Institute of Bioinformatics, International Tech Park, Bangalore, India.
  • Nunia V; Manipal Academy of Higher Education, Manipal, India.
  • Nagappa M; Neuromuscular Laboratory, Neurobiology Research Centre (NRC), National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India.
  • Sinha S; Department of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India.
  • Khanna T; Genetic Metabolic Disorders Service, Children's Hospital at Westmead, Sydney, NSW, Australia.
  • Thangaraj K; Neuromuscular Laboratory, Neurobiology Research Centre (NRC), National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India.
  • Taly AB; Department of Clinical Neurosciences, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India.
  • Gayathri N; Department of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India.
J Mol Neurosci ; 71(11): 2219-2228, 2021 Nov.
Article em En | MEDLINE | ID: mdl-33469851
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Doenças Mitocondriais / DNA Polimerase gama / Mutação Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Doenças Mitocondriais / DNA Polimerase gama / Mutação Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article