(Q31024326)

English

Clinical and ERG data in a family with autosomal dominant RP and Pro-347-Arg mutation in the rhodopsin gene

scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 June 2017

Clinical and ERG data in a family with autosomal dominant RP and Pro-347-Arg mutation in the rhodopsin gene (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 June 2017

author name string

Niemeyer G

1

1 reference

Europe PubMed Central

PubMed publication ID

28 June 2017

Trüb P

2

1 reference

Europe PubMed Central

PubMed publication ID

28 June 2017

Schinzel A

3

1 reference

Europe PubMed Central

PubMed publication ID

28 June 2017

Gal A

4

1 reference

Europe PubMed Central

PubMed publication ID

28 June 2017

publication date

1 January 1992

1 reference

Europe PubMed Central

PubMed publication ID

28 June 2017

Documenta Ophthalmologica

1 reference

Europe PubMed Central

PubMed publication ID

28 June 2017

79

1 reference

Europe PubMed Central

PubMed publication ID

28 June 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

28 June 2017

303-311

1 reference

Europe PubMed Central

PubMed publication ID

28 June 2017

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

1 reference

https://api.crossref.org/works/10.1007%2FBF00160945

21 January 2018

ERG in Behçet's disease (author's transl)

1 reference

https://pubmed.ncbi.nlm.nih.gov/1633742

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1633742

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Refractive errors of retinitis pigmentosa patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/1633742

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A 3-bp deletion in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/1633742

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/1633742

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/1633742

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ocular findings in patients with autosomal dominant retinitis pigmentosa and rhodopsin, proline-347-leucine

1 reference

https://pubmed.ncbi.nlm.nih.gov/1633742

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Electroretinography: Some basic principles

1 reference

https://pubmed.ncbi.nlm.nih.gov/1633742

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unusual electroretinograms

1 reference

https://pubmed.ncbi.nlm.nih.gov/1633742

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two forms of autosomal dominant primary retinitis pigmentosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/1633742

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pro-347-Arg mutation of the rhodopsin gene in autosomal dominant retinitis pigmentosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/1633742

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1633742

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant retinitis pigmentosa. A method of classification

1 reference

https://pubmed.ncbi.nlm.nih.gov/1633742

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Degenerative changes in a retina affected with autosomal dominant retinitis pigmentosa.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1633742

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rod and cone activity in patients with dominantly inherited retinitis pigmentosa: comparisons between psychophysical and electroretinographic measurements

1 reference

https://pubmed.ncbi.nlm.nih.gov/1633742

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00160945

1 reference

Europe PubMed Central

PubMed publication ID

28 June 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 June 2017

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