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Generation of an iPSC line (RMCGENi020-A) from a patient with Stargardt disease harboring the recurrent intronic ABCA4 variant c.4253+43G>A.
Suárez-Herrera, Nuria; Leijsten, Nico; Albert, Silvia; Bax, Nathalie M; Hoyng, Carel B; Cremers, Frans P M; Garanto, Alejandro; Collin, Rob W J.
Afiliación
  • Suárez-Herrera N; Radboud University Medical Center, Department of Human Genetics, Nijmegen, the Netherlands.
  • Leijsten N; Radboud University Medical Center, Department of Human Genetics, Nijmegen, the Netherlands.
  • Albert S; Radboud University Medical Center, Department of Human Genetics, Nijmegen, the Netherlands.
  • Bax NM; Radboud University Medical Center, Department of Ophthalmology, Nijmegen, the Netherlands.
  • Hoyng CB; Radboud University Medical Center, Department of Ophthalmology, Nijmegen, the Netherlands.
  • Cremers FPM; Radboud University Medical Center, Department of Human Genetics, Nijmegen, the Netherlands.
  • Garanto A; Radboud University Medical Center, Department of Human Genetics, Nijmegen, the Netherlands; Amalia Children's Hospital, Department of Pediatrics, Nijmegen, the Netherlands.
  • Collin RWJ; Radboud University Medical Center, Department of Human Genetics, Nijmegen, the Netherlands. Electronic address: rob.collin@radboudumc.nl.
Stem Cell Res ; 73: 103252, 2023 12.
Article en En | MEDLINE | ID: mdl-37979432
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Células Madre Pluripotentes Inducidas / Enfermedad de Stargardt Límite: Humans Idioma: En Revista: Stem Cell Res Año: 2023 Tipo del documento: Article País de afiliación: Países Bajos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Células Madre Pluripotentes Inducidas / Enfermedad de Stargardt Límite: Humans Idioma: En Revista: Stem Cell Res Año: 2023 Tipo del documento: Article País de afiliación: Países Bajos