(Q34389589)

1 August 2017

A new locus for autosomal dominant stargardt-like disease maps to chromosome 4. (English)

1 reference

1 August 2017

Kniazeva M

1

1 reference

1 August 2017

Chiang MF

2

1 reference

1 August 2017

Morgan B

3

1 reference

1 August 2017

Anduze AL

4

1 reference

1 August 2017

Zack DJ

5

1 reference

1 August 2017

Han M

6

1 reference

1 August 2017

Zhang K

7

1 reference

1 August 2017

language of work or name

English

0 references

publication date

1 May 1999

1 reference

American Journal of Human Genetics

1 August 2017

1 reference

1 August 2017

64

1 reference

1 August 2017

1394-1399

1 reference

1 August 2017

5

1 reference

Sequential tests for the detection of linkage

1 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377876

A physical map of 30,000 human genes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377876

Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degeneration

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377876

A mutation in guanylate cyclase activator 1A (GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21.1

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377876

Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377876

Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377876

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377876

A novel gene family defined by human dihydropyrimidinase and three related proteins with differential tissue distribution

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377876

Expression of heat shock proteins in the developing rat retina.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377876

A comprehensive genetic map of the human genome based on 5,264 microsatellites

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377876

Genetic linkage of cone-rod retinal dystrophy to chromosome 19q and evidence for segregation distortion

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377876

Sibling correlations and segregation analysis of age-related maculopathy: the Beaver Dam Eye Study.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377876

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377876

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377876

The dark choroid in posterior retinal dystrophies

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377876

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377876

Pathophysiology of age-related macular degeneration

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377876

Nucleotide sequence and regulation of a human 90-kDa heat shock protein gene

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377876

Autosomal-dominant fundus flavimaculatus. Clinicopathologic correlation

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377876

Fundus Flavimaculatus and Stargardt's Disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377876

Stargardt's Disease and Fundus Flavimaculatus

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377876

A gene for Stargardt's disease (fundus flavimaculatus) maps to the short arm of chromosome 1

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377876

Familial aggregation of age-related maculopathy.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377876

Allelic variation in ABCR associated with Stargardt disease but not age-related macular degeneration

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377876

Dominantly inherited macular dystrophy with flecks (Stargardt)

9 December 2018

1 reference

12 December 2020

Age-related macular degeneration

1 reference

12 December 2020

Long-term follow-up of dominant macular dystrophy with flecks (Stargardt)

1 reference

12 December 2020

Mapping of autosomal dominant cone degeneration to chromosome 17p

1 reference

12 December 2020

A prospective study of cigarette smoking and age-related macular degeneration in women

1 reference

12 December 2020

Localisation of a gene for dominant cone-rod dystrophy (CORD6) to chromosome 17p

1 reference

12 December 2020

ABCR unites what ophthalmologists divide(s)

1 reference

12 December 2020

Fundus flavimaculatus. A clinical classification

1 reference

12 December 2020

Identifiers

DOI

10.1086/302377

1 reference

1 August 2017

1 reference

1 August 2017

1 reference