NEW ANIMAL ACHROMATOPSIA MODEL

The present invention describes non-consanguineous albino HsdWin:NMRI mice, which are mutant for the Gnat2 gene, which causes the damaged coneless retina phenotype, preferably a Gnat2cpf13 mutation, and more preferably in homozygosis. The present invention also relates to the use of said mice, speci...

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Main Authors MONTOLIU JOSE, LLUIS, ZURITA REDONDO, MARIA ESTHER, DE LA VILLA POLO, PEDRO, BENITEZ ORTIZ, JAVIER, GONZALEZ NEIRA, ANNA, FERNANDEZ LOPEZ, ALMUDENA
Format Patent
LanguageEnglish
French
Spanish
Published 20.02.2014
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