(Q28307487)

2

0 references

R E Ferrell

3

0 references

V C Sheffield

4

0 references

S G Jacobson

5

0 references

J D Gass

6

0 references

E Mitchell

7

0 references

E M Stone

Photoreceptor peripherin is the normal product of the gene responsible for retinal degeneration in the rds mouse

8

0 references

language of work or name

English

0 references

publication date

February 1995

0 references

published in

Ophthalmology

0 references

volume

102

0 references

issue

2

0 references

page(s)

246-55

0 references

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2931029-9

7 January 2021

A point mutation of the rhodopsin gene in one form of retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2931029-9

7 January 2021

Ocular findings in patients with autosomal dominant retinitis pigmentosa and a rhodopsin gene defect (Pro-23-His).

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2931029-9

7 January 2021

Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2931029-9

7 January 2021

A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2931029-9

7 January 2021

Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2931029-9

7 January 2021

Butterfly-shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2931029-9

7 January 2021

A null mutation in the human peripherin/RDS gene in a family with autosomal dominant retinitis punctata albescens

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2931029-9

7 January 2021

The retinal degeneration slow (rds) gene product is a photoreceptor disc membrane-associated glycoprotein.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2931029-9

7 January 2021

Phenotypic Variation Including Retinitis Pigmentosa, Pattern Dystrophy, and Fundus Flavimaculatus in a Single Family With a Deletion of Codon 153 or 154 of the Peripherin/RDS Gene

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2931029-9

7 January 2021

Protocols for an improved detection of point mutations by SSCP

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2931029-9

7 January 2021

An electroretinographic and molecular genetic study of X-linked cone degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2931029-9

7 January 2021

A dominant Stargardt's macular dystrophy locus maps to chromosome 13q34

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2931029-9

7 January 2021

Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6q

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2931029-9

7 January 2021

Pathophysiology of age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2931029-9

7 January 2021

Age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2931029-9

7 January 2021