Your browser doesn't support javascript.
loading
Clinical and genetic analysis of Indian patients with NDP-related retinopathies.
Sudha, Dhandayuthapani; Ganapathy, Aparna; Mohan, Puja; Mannan, Ashraf U; Krishna, Shuba; Neriyanuri, Srividya; Swaminathan, Meenakshi; Rishi, Pukhraj; Chidambaram, Subbulakshmi; Arunachalam, Jayamuruga Pandian.
  • Sudha D; SN ONGC Department of Genetics and Molecular Biology, Vision Research Foundation, 41, College Road, Nungambakkam, Chennai, 600006, India.
  • Ganapathy A; School of Biotechnology, SASTRA University, Thanjavur, India.
  • Mohan P; Strand Life Sciences, Hebbal, Bengaluru, India.
  • Mannan AU; Strand Life Sciences, Hebbal, Bengaluru, India.
  • Krishna S; Strand Life Sciences, Hebbal, Bengaluru, India.
  • Neriyanuri S; Strand Life Sciences, Hebbal, Bengaluru, India.
  • Swaminathan M; Elite School of Optometry, Unit of Medical Research Foundation, Chennai, India.
  • Rishi P; Department of Pediatric Ophthalmology, Medical Research Foundation, Chennai, India.
  • Chidambaram S; Shri Bhagwan Mahavir Vitreo-Retinal Services, Sankara Nethralaya, Medical Research Foundation, Chennai, India.
  • Arunachalam JP; R.S. Mehta Jain Department of Biochemistry and Cell Biology, Vision Research Foundation, Chennai, India.
Int Ophthalmol ; 38(3): 1251-1260, 2018 Jun.
Article en En | MEDLINE | ID: mdl-28602015

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Retina / Enfermedades de la Retina / Espasmos Infantiles / Anomalías Múltiples / ADN / Ceguera / Mutación Missense / Enfermedades Genéticas Ligadas al Cromosoma X / Proteínas del Ojo / Proteínas del Tejido Nervioso Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Retina / Enfermedades de la Retina / Espasmos Infantiles / Anomalías Múltiples / ADN / Ceguera / Mutación Missense / Enfermedades Genéticas Ligadas al Cromosoma X / Proteínas del Ojo / Proteínas del Tejido Nervioso Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Año: 2018 Tipo del documento: Article