(Q34297104)

English

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

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

author name string

Horn M

1

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Humphries P

2

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Kunisch M

3

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Marchese C

4

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Apfelstedt-Sylla E

5

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Fugi L

6

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Zrenner E

7

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Kenna P

8

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Gal A

9

1 reference

Europe PubMed Central

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1 August 2017

Farrar J

10

1 reference

Europe PubMed Central

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1 August 2017

publication date

1 November 1992

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Europe PubMed Central

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1 August 2017

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

90

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Europe PubMed Central

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1 August 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

255-257

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

https://scigraph.springernature.com/pub.10.1007/bf00220073

0 references

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1487240

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/1487240

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

1 reference

https://pubmed.ncbi.nlm.nih.gov/1487240

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rhodopsin mutations in autosomal dominant retinitis pigmentosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/1487240

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regulation of transmembrane signaling by receptor phosphorylation

1 reference

https://pubmed.ncbi.nlm.nih.gov/1487240

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/1487240

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant retinitis pigmentosa: Four new mutations in rhodopsin, one of them in the retinal attachment site

1 reference

https://pubmed.ncbi.nlm.nih.gov/1487240

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/1487240

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/1487240

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of novel rhodopsin mutations associated with retinitis pigmentosa by GC-clamped denaturing gradient gel electrophoresis

1 reference

https://pubmed.ncbi.nlm.nih.gov/1487240

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mechanism of rhodopsin kinase activation

1 reference

https://pubmed.ncbi.nlm.nih.gov/1487240

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid detection of single base mismatches as heteroduplexes on Hydrolink gels

1 reference

https://pubmed.ncbi.nlm.nih.gov/1487240

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00220073

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

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