(Q73816552)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9342608%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

title

Ocular findings in patients with autosomal dominant retinitis pigmentosa and Cys110Phe, Arg135Gly, and Gln344stop mutations of rhodopsin (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9342608%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference

7

1 reference

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6 November 2019

author name string

S Kremmer

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9342608%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

A Eckstein

2

1 reference

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6 November 2019

A Gal

3

1 reference

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6 November 2019

E Apfelstedt-Sylla

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9342608%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

H Wedemann

5

1 reference

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6 November 2019

K Rüther

6

1 reference

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6 November 2019

publication date

1 September 1997

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9342608%20AND%20SRC:MED&resulttype=core&format=json

Graefe's Archive for Clinical and Experimental Ophthalmology

6 November 2019

published in

1 reference

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6 November 2019

volume

235

1 reference

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6 November 2019

issue

9

1 reference

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6 November 2019

page(s)

575-583

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf00947087

6 November 2019

exact match

0 references

cites work

Improved electrode for electroretinography

1 reference

12 December 2020

Cysteine residues 110 and 187 are essential for the formation of correct structure in bovine rhodopsin

1 reference

12 December 2020

Ocular findings in a family with autosomal dominant retinitis pigmentosa and a frameshift mutation altering the carboxyl terminal sequence of rhodopsin.

1 reference

12 December 2020

Dominant retinitis pigmentosa associated with two rhodopsin gene mutations. Leu-40-Arg and an insertion disrupting the 5'-splice junction of exon 5.

1 reference

12 December 2020

Retinal function and rhodopsin levels in autosomal dominant retinitis pigmentosa with rhodopsin mutations

1 reference

12 December 2020

A rhodopsin gene mutation responsible for autosomal dominant retinitis pigmentosa results in a protein that is defective in localization to the photoreceptor outer segment

1 reference

12 December 2020

Doyne Lecture. Rhodopsin and autosomal dominant retinitis pigmentosa

1 reference

12 December 2020

Identification of novel rhodopsin mutations responsible for retinitis pigmentosa: implications for the structure and function of rhodopsin

1 reference

12 December 2020

Molecular Analysis and Genetic Mapping of the Rhodopsin Gene in Families with Autosomal Dominant Retinitis Pigmentosa

1 reference

12 December 2020

Three novel rhodopsin mutations (C110F, L131P, A164V) in patients with autosomal dominant retinitis pigmentosa

1 reference

12 December 2020

Two forms of autosomal dominant primary retinitis pigmentosa

1 reference

12 December 2020

Clinical expression correlates with location of rhodopsin mutation in dominant retinitis pigmentosa

1 reference

12 December 2020

Deletions in exon 5 of the human rhodopsin gene causing a shift in the reading frame and autosomal dominant retinitis pigmentosa

1 reference

12 December 2020

[Clinical electroretinography: standard protocol and normal values]

1 reference

12 December 2020

Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa

1 reference

12 December 2020

Autosomal dominant retinitis pigmentosa. A method of classification

1 reference

12 December 2020

Standard for clinical electroretinography (1994 update)

1 reference

12 December 2020

Autosomal dominant sectoral retinitis pigmentosa. Two families with transversion mutation in codon 23 of rhodopsin

1 reference

12 December 2020