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Generation of a human iPSC line, INMi002-A, carrying the most prevalent USH2A variant associated with Usher syndrome type 2.
Sanjurjo-Soriano, Carla; Erkilic, Nejla; Manes, Gaël; Dubois, Gregor; Hamel, Christian P; Meunier, Isabelle; Kalatzis, Vasiliki.
  • Sanjurjo-Soriano C; Inserm U1051, Institute for Neurosciences of Montpellier, Montpellier, France; University of Montpellier, Montpellier, France.
  • Erkilic N; Inserm U1051, Institute for Neurosciences of Montpellier, Montpellier, France; University of Montpellier, Montpellier, France.
  • Manes G; Inserm U1051, Institute for Neurosciences of Montpellier, Montpellier, France; University of Montpellier, Montpellier, France.
  • Dubois G; Inserm U1051, Institute for Neurosciences of Montpellier, Montpellier, France; University of Montpellier, Montpellier, France.
  • Hamel CP; Inserm U1051, Institute for Neurosciences of Montpellier, Montpellier, France; University of Montpellier, Montpellier, France; Centre of Reference for Genetic Sensory Diseases, CHU, Montpellier, France.
  • Meunier I; Inserm U1051, Institute for Neurosciences of Montpellier, Montpellier, France; University of Montpellier, Montpellier, France; Centre of Reference for Genetic Sensory Diseases, CHU, Montpellier, France.
  • Kalatzis V; Inserm U1051, Institute for Neurosciences of Montpellier, Montpellier, France; University of Montpellier, Montpellier, France. Electronic address: vasiliki.kalatzis@inserm.fr.
Stem Cell Res ; 33: 247-250, 2018 12.
Article en En | MEDLINE | ID: mdl-30468996

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndromes de Usher / Células Madre Pluripotentes Inducidas Tipo de estudio: Risk_factors_studies Límite: Female / Humans / Middle aged Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndromes de Usher / Células Madre Pluripotentes Inducidas Tipo de estudio: Risk_factors_studies Límite: Female / Humans / Middle aged Idioma: En Año: 2018 Tipo del documento: Article