(Q33681302)

28 July 2017

title

Fine localisation of the gene for central areolar choroidal dystrophy on chromosome 17p. (English)

1 reference

28 July 2017

Hughes AE

1

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28 July 2017

Lotery AJ

series ordinal

2

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28 July 2017

Silvestri G

series ordinal

3

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28 July 2017

language of work or name

English

0 references

publication date

1 September 1998

1 reference

Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

35

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28 July 2017

issue

9

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28 July 2017

page(s)

770-772

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The retina: genetic studies of several retinopathies located on the short arm of chromosome 17.

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051432

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051432

Localization of Drosophila retinal degeneration B, a membrane-associated phosphatidylinositol transfer protein

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051432

A new locus for autosomal dominant retinitis pigmentosa on the short arm of chromosome 17.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051432

Chromosome mapping of the human arrestin (SAG), beta-arrestin 2 (ARRB2), and beta-adrenergic receptor kinase 2 (ADRBK2) genes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051432

Localisation of a gene for central areolar choroidal dystrophy to chromosome 17p.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051432

Evidence of genetic heterogeneity of Leber's congenital amaurosis (LCA) and mapping of LCA1 to chromosome 17p13.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051432

A gene for autosomal dominant progressive cone dystrophy (CORD5) maps to chromosome 17p12-p13

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051432

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

10 December 2018

1 reference

12 December 2020

The effect of recoverin-like calcium-binding proteins on the photoresponse of retinal rods

1 reference

12 December 2020

A locus for autosomal dominant anterior polar cataract on chromosome 17p

1 reference

12 December 2020

Expression, secretion, and age-related downregulation of pigment epithelium-derived factor, a serpin with neurotrophic activity

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.35.9.770

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28 July 2017

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28 July 2017

1 reference