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 | , , , , , |
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Format | Patent |
Language | English French Spanish |
Published |
20.02.2014
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Subjects | |
Online Access | Get full text |
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