(Q33680285)

28 July 2017

RP11 is the second most common locus for dominant retinitis pigmentosa (English)

1 reference

28 July 2017

1 reference

Vithana E

1

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28 July 2017

Al-Maghtheh M

series ordinal

2

1 reference

28 July 2017

Bhattacharya SS

series ordinal

3

1 reference

28 July 2017

Inglehearn CF

series ordinal

4

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 February 1998

1 reference

Journal of Medical Genetics

28 July 2017

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28 July 2017

35

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28 July 2017

2

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28 July 2017

174-175

1 reference

A linkage survey of 20 dominant retinitis pigmentosa families: frequencies of the nine known loci and evidence for further heterogeneity

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051233

Complement and complement regulatory proteins in human tears.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051233

Evidence for a major retinitis pigmentosa locus on 19q13.4 (RP11) and association with a unique bimodal expressivity phenotype

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051233

Simple tests for rhodopsin involvement in retinitis pigmentosa

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051233

A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051233

Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051233

Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051233

14 July 2018

Identifiers

DOI

10.1136/JMG.35.2.174-A

1 reference

28 July 2017

1 reference

28 July 2017

1 reference