Preferential silencing of a common dominant rhodopsin mutation does not inhibit retinal degeneration in a transgenic model (Q58413953)

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30 December 2019

title

Preferential silencing of a common dominant rhodopsin mutation does not inhibit retinal degeneration in a transgenic model (English)

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30 December 2019

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3

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30 December 2019

Luciano Domenici

6

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30 December 2019

Alberto Auricchio

8

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4

Mariacarmela Allocca

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30 December 2019

author name string

Alessandra Tessitore

1

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30 December 2019

Fabiana Parisi

2

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30 December 2019

Umberto Di Vicino

5

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Irene Bozzoni

7

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publication date

18 September 2006

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30 December 2019

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volume

14

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30 December 2019

issue

5

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30 December 2019

page(s)

692-699

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Gene mutations in retinitis pigmentosa and their clinical implications

30 December 2019

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The nature of dominant mutations of rhodopsin and implications for gene therapy

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Focus on molecules: rhodopsin

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A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa

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A rhodopsin mutant linked to autosomal dominant retinitis pigmentosa is prone to aggregate and interacts with the ubiquitin proteasome system

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Identifiers

DOI

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30 December 2019

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