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Cav1.4 dysfunction and congenital stationary night blindness type 2.
Koschak, Alexandra; Fernandez-Quintero, Monica L; Heigl, Thomas; Ruzza, Marco; Seitter, Hartwig; Zanetti, Lucia.
  • Koschak A; Institute of Pharmacy, Pharmacology and Toxicology, Center for Chemistry and Biomedicine, University of Innsbruck, Innrain 80-82/III, 6020, Innsbruck, Austria. alexandra.koschak@uibk.ac.at.
  • Fernandez-Quintero ML; Institute of General, Inorganic and Theoretical Chemistry, Center for Chemistry and Biomedicine, University of Innsbruck, Innrain 80-82/III, 6020, Innsbruck, Austria.
  • Heigl T; Institute of Pharmacy, Pharmacology and Toxicology, Center for Chemistry and Biomedicine, University of Innsbruck, Innrain 80-82/III, 6020, Innsbruck, Austria.
  • Ruzza M; Institute of Pharmacy, Pharmacology and Toxicology, Center for Chemistry and Biomedicine, University of Innsbruck, Innrain 80-82/III, 6020, Innsbruck, Austria.
  • Seitter H; Institute of Pharmacy, Pharmacology and Toxicology, Center for Chemistry and Biomedicine, University of Innsbruck, Innrain 80-82/III, 6020, Innsbruck, Austria.
  • Zanetti L; Institute of Pharmacy, Pharmacology and Toxicology, Center for Chemistry and Biomedicine, University of Innsbruck, Innrain 80-82/III, 6020, Innsbruck, Austria.
Pflugers Arch ; 473(9): 1437-1454, 2021 09.
Article en En | MEDLINE | ID: mdl-34212239
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Hereditarias del Ojo / Ceguera Nocturna / Canales de Calcio Tipo L / Enfermedades Genéticas Ligadas al Cromosoma X / Miopía Límite: Animals / Humans Idioma: En Año: 2021 Tipo del documento: Article
Texto completo
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Hereditarias del Ojo / Ceguera Nocturna / Canales de Calcio Tipo L / Enfermedades Genéticas Ligadas al Cromosoma X / Miopía Límite: Animals / Humans Idioma: En Año: 2021 Tipo del documento: Article