(Q54793818)

3 June 2018

title

A Swedish family with a mutation in the peripherin/RDS gene (Arg-172-Trp) associated with a progressive retinal degeneration. (English)

1 reference

3 June 2018

0 references

Ekström U

1

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3 June 2018

Andréasson S

2

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3 June 2018

Ponjavic V

3

1 reference

3 June 2018

Abrahamson M

4

1 reference

3 June 2018

Sandgren O

5

1 reference

3 June 2018

Nilsson-Ehle P

6

1 reference

3 June 2018

Ehinger B

7

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3 June 2018

publication date

1 September 1998

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3 June 2018

published in

Ophthalmic Genetics

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3 June 2018

volume

19

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3 June 2018

page(s)

149-156

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3 June 2018

issue

3

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3 June 2018

DNA sequencing with chain-terminating inhibitors

cites work

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.19.3.149.2186

A peripherin/retinal degeneration slow mutation (Pro-210-Arg) associated with macular and peripheral retinal degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.19.3.149.2186

Autosomal dominant retinitis pigmentosa: a novel mutation at the peripherin/RDS locus in the original 6p-linked pedigree

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.19.3.149.2186

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.19.3.149.2186

Full characterization of the maculopathy associated with an Arg-172-Trp mutation in the RDS/peripherin gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.19.3.149.2186

10.1076/OPGE.19.3.149.2186

21 January 2018

Identifiers

DOI

1 reference

3 June 2018

PubMed ID

9810570

1 reference

3 June 2018