(Q24517958)

English

Assessment of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene localised to 6q13-q15 in autosomal dominant Stargardt-like disease (ADSTGD), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1).

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

2 July 2017

Assessment of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene localised to 6q13-q15 in autosomal dominant Stargardt-like disease (ADSTGD), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1). (English)

1 reference

Europe PubMed Central

2 July 2017

North Carolina macular dystrophy

1 reference

based on heuristic

inferred from title

progressive bifocal chorioretinal atrophy

1 reference

based on heuristic

inferred from title

author name string

Gehrig A

1

author given names

A

author last names

Gehrig

1 reference

Europe PubMed Central

2 July 2017

Felbor U

2

author given names

U

author last names

Felbor

1 reference

Europe PubMed Central

2 July 2017

Kelsell RE

3

author given names

R E

author last names

Kelsell

1 reference

Europe PubMed Central

2 July 2017

Hunt DM

4

author given names

D M

author last names

Hunt

1 reference

Europe PubMed Central

2 July 2017

Maumenee IH

5

author given names

I H

author last names

Maumenee

1 reference

Europe PubMed Central

2 July 2017

Weber BH

6

author given names

B H

author last names

Weber

1 reference

Europe PubMed Central

2 July 2017

language of work or name

0 references

publication date

1 August 1998

1 reference

Europe PubMed Central

2 July 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

2 July 2017

35

1 reference

Europe PubMed Central

2 July 2017

641-645

1 reference

Europe PubMed Central

2 July 2017

8

1 reference

Europe PubMed Central

2 July 2017

A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051388

7 April 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051388

7 April 2017

Retinal-specific guanylate cyclase gene mutations in Leber's congenital amaurosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051388

24 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051388

24 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051388

24 March 2017

Mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) in patients with Sorsby's fundus dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051388

24 March 2017

An ancestral core haplotype defines the critical region harbouring the North Carolina macular dystrophy gene (MCDR1).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051388

27 September 2017

Progressive bifocal chorio-retinal atrophy. A rare familial disease of the eyes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051388

27 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051388

27 September 2017

Rod and cone specific domains in the interphotoreceptor matrix

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051388

27 September 2017

Autosomal-dominant fundus flavimaculatus. Clinicopathologic correlation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051388

30 May 2018

Comparison of photoreceptor-specific matrix domains in the cat and monkey retinas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051388

30 May 2018

Xyloside-induced disruption of interphotoreceptor matrix proteoglycans results in retinal detachment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051388

30 May 2018

Localization of the gene for progressive bifocal chorioretinal atrophy (PBCRA) to chromosome 6q

1 reference

https://pubmed.ncbi.nlm.nih.gov/9719369

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

North Carolina macular dystrophy is assigned to chromosome 6

1 reference

https://pubmed.ncbi.nlm.nih.gov/9719369

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The interphotoreceptor matrix mediates primate retinal adhesion

1 reference

https://pubmed.ncbi.nlm.nih.gov/9719369

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Positional cloning moves from perditional to traditional

1 reference

https://pubmed.ncbi.nlm.nih.gov/9719369

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and genetic evidence for autosomal dominant North Carolina macular dystrophy in a German family

1 reference

https://pubmed.ncbi.nlm.nih.gov/9719369

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interphotoreceptor matrix domains ensheath vertebrate cone photoreceptor cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/9719369

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Insoluble interphotoreceptor matrix domains surround rod photoreceptors in the human retina

1 reference

https://pubmed.ncbi.nlm.nih.gov/9719369

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical features of progressive bifocal chorioretinal atrophy: a retinal dystrophy linked to chromosome 6q

1 reference

https://pubmed.ncbi.nlm.nih.gov/9719369

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnostic single strand conformational polymorphism, (SSCP): a simplified non-radioisotopic method as applied to a Tay-Sachs B1 variant

1 reference

https://api.crossref.org/works/10.1136%2FJMG.35.8.641

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1136/JMG.35.8.641

1 reference

Europe PubMed Central

2 July 2017

release_p64w34fianh6xacwavic2o4fby

0 references

0 references

1 reference

Europe PubMed Central

2 July 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q24517958&oldid=1999321492"