Your browser doesn't support javascript.
loading
A ROD-CONE DYSTROPHY IS SYSTEMATICALLY ASSOCIATED TO THE RTN4IP1 RECESSIVE OPTIC ATROPHY.
Meunier, Isabelle; Bocquet, Béatrice; Charif, Majida; Dhaenens, Claire-Marie; Manes, Gael; Amati-Bonneau, Patrizia; Roubertie, Agathe; Zanlonghi, Xavier; Lenaers, Guy.
Afiliación
  • Meunier I; Institute for Neurosciences of Montpellier U1051, University of Montpellier, Montpellier, France.
  • Bocquet B; National Center in Rare Diseases, Genetics of Sensory Diseases, University Hospital, Montpellier, France.
  • Charif M; Institute for Neurosciences of Montpellier U1051, University of Montpellier, Montpellier, France.
  • Dhaenens CM; National Center in Rare Diseases, Genetics of Sensory Diseases, University Hospital, Montpellier, France.
  • Manes G; Genetics, and Immuno-cell Therapy Team, Mohammed First University, Oujda, Morocco.
  • Amati-Bonneau P; Biochemistry and Molecular Biology Department-UF Génopathies, Univ Lille, Lille, France.
  • Roubertie A; Institute for Neurosciences of Montpellier U1051, University of Montpellier, Montpellier, France.
  • Zanlonghi X; Department of Biochemistry and Genetics, University Hospital Angers, Angers, France.
  • Lenaers G; Institute for Neurosciences of Montpellier U1051, University of Montpellier, Montpellier, France.
Retina ; 41(8): 1771-1779, 2021 Aug 01.
Article en En | MEDLINE | ID: mdl-33315831
Asunto(s)
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: ADN / Proteínas Portadoras / Proteínas Mitocondriales / Distrofias de Conos y Bastones / Mutación Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Idioma: En Revista: Retina Año: 2021 Tipo del documento: Article País de afiliación: Francia
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: ADN / Proteínas Portadoras / Proteínas Mitocondriales / Distrofias de Conos y Bastones / Mutación Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Idioma: En Revista: Retina Año: 2021 Tipo del documento: Article País de afiliación: Francia