(Q54348665)

28 May 2018

title

Oguchi disease masked by retinitis pigmentosa. (English)

1 reference

28 May 2018

author name string

Hiroko Sonoyama

1

1 reference

28 May 2018

Kei Shinoda

2

1 reference

28 May 2018

Chie Ishigami

3

1 reference

28 May 2018

Yumi Tada

4

1 reference

28 May 2018

Hidenao Ideta

5

1 reference

28 May 2018

Ryuichi Ideta

6

1 reference

28 May 2018

Masayo Takahashi

7

1 reference

28 May 2018

Yozo Miyake

8

1 reference

28 May 2018

publication date

16 September 2011

1 reference

28 May 2018

Documenta Ophthalmologica

published in

1 reference

28 May 2018

volume

123

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28 May 2018

issue

2

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28 May 2018

page(s)

127-133

1 reference

28 May 2018

https://scigraph.springernature.com/pub.10.1007/s10633-011-9286-x

exact match

0 references

cites work

A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese

1 reference

https://api.crossref.org/works/10.1007%2FS10633-011-9286-X

Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10633-011-9286-X

The photopic hill: a new phenomenon of the light adapted electroretinogram

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10633-011-9286-X

Novel mutations in the arrestin gene and associated clinical features in Japanese patients with Oguchi's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10633-011-9286-X

Gene analysis and evaluation of the single founder effect in Japanese patients with Oguchi disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10633-011-9286-X

Visual function and gene analysis in a family with Oguchi's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10633-011-9286-X

The structural basis of arrestin-mediated regulation of G-protein-coupled receptors

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10633-011-9286-X

Retinitis pigmentosa with visual fluctuation and arrestin gene mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10633-011-9286-X

Oguchi disease: phenotypic characteristics of patients with the frequent 1147delA mutation in the arrestin gene

21 January 2018

1 reference

12 December 2020

Oguchi disease with sectoral retinitis pigmentosa harboring adenine deletion at position 1147 in the arrestin gene

1 reference

12 December 2020

Arrestin gene mutations in autosomal recessive retinitis pigmentosa

1 reference

12 December 2020

Two Indian siblings with Oguchi disease are homozygous for an arrestin mutation encoding premature termination

1 reference

12 December 2020

Electrophysiological findings in patients with Oguchi's disease

1 reference

12 December 2020

Histologic study of Oguchi's disease. Its relationship to pigmentary degeneration of the retina

1 reference

12 December 2020

Macular Dysfunction in Oguchi Disease with the Frequent Mutation 1147delA in the SAG Gene

1 reference

12 December 2020

10.1007/S10633-011-9286-X

Identifiers

DOI

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/dey57oisqvbdtk6zzzgoxqa7g4

30 July 2022

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Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/dey57oisqvbdtk6zzzgoxqa7g4

30 July 2022

mapped directly with Wikidata item

https://api.fatcat.wiki/v0/release/dey57oisqvbdtk6zzzgoxqa7g4

1 reference

30 July 2022