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Leber's Hereditary Optic Neuropathy-Specific Mutation m.11778G>A Exists on Diverse Mitochondrial Haplogroups in India.
Khan, Nahid Akhtar; Govindaraj, Periyasamy; Soumittra, Nagasamy; Sharma, Sonika; Srilekha, Sundaramoorthy; Ambika, Selvakumar; Vanniarajan, Ayyasamy; Meena, Angamuthu Kanikannan; Uppin, Megha S; Sundaram, Challa; Bindu, Parayil Sankaran; Gayathri, Narayanappa; Taly, Arun B; Thangaraj, Kumarasamy.
Afiliação
  • Khan NA; Council of Scientific and Industrial Research, Centre for Cellular and Molecular Biology, Hyderabad, India.
  • Govindaraj P; Council of Scientific and Industrial Research, Centre for Cellular and Molecular Biology, Hyderabad, India 2Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India 3Neuromuscular Laboratory, Neurobiology Research Centre, National Institute of Mental Health an
  • Soumittra N; SNONGC Department of Genetics and Molecular Biology, Vision Research Foundation, Sankara Nethralaya, Chennai, India.
  • Sharma S; Council of Scientific and Industrial Research, Centre for Cellular and Molecular Biology, Hyderabad, India.
  • Srilekha S; SNONGC Department of Genetics and Molecular Biology, Vision Research Foundation, Sankara Nethralaya, Chennai, India.
  • Ambika S; Department of Neuro-Ophthalmology, Medical Research Foundation, Sankara Nethralaya Chennai, India.
  • Vanniarajan A; Council of Scientific and Industrial Research, Centre for Cellular and Molecular Biology, Hyderabad, India 6Department of Molecular Genetics, Aravind Medical Research Foundation, Madurai, India.
  • Meena AK; Department of Neurology, Nizam's Institute of Medical Sciences, Hyderabad, India.
  • Uppin MS; Department of Pathology, Nizam's Institute of Medical Sciences, Hyderabad, India.
  • Sundaram C; Department of Pathology, Nizam's Institute of Medical Sciences, Hyderabad, India.
  • Bindu PS; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India 3Neuromuscular Laboratory, Neurobiology Research Centre, National Institute of Mental Health and Neurosciences, Bengaluru, India.
  • Gayathri N; Neuromuscular Laboratory, Neurobiology Research Centre, National Institute of Mental Health and Neurosciences, Bengaluru, India 9Department of Neuropathology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
  • Taly AB; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India 3Neuromuscular Laboratory, Neurobiology Research Centre, National Institute of Mental Health and Neurosciences, Bengaluru, India.
  • Thangaraj K; Council of Scientific and Industrial Research, Centre for Cellular and Molecular Biology, Hyderabad, India.
Invest Ophthalmol Vis Sci ; 58(10): 3923-3930, 2017 08 01.
Article em En | MEDLINE | ID: mdl-28768321
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA Mitocondrial / Mutação Puntual / Atrofia Óptica Hereditária de Leber / Povo Asiático / NADH Desidrogenase Limite: Adult / Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: Invest Ophthalmol Vis Sci Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Índia País de publicação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA Mitocondrial / Mutação Puntual / Atrofia Óptica Hereditária de Leber / Povo Asiático / NADH Desidrogenase Limite: Adult / Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: Invest Ophthalmol Vis Sci Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Índia País de publicação: Estados Unidos