(Q44467516)

3 December 2017

title

Phenotype in two families with RP3 associated with RPGR mutations (English)

1 reference

3 December 2017

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Birgit Lorenz

1

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3 December 2017

Monika Andrassi

series ordinal

2

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3 December 2017

Ulf Kretschmann

series ordinal

3

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3 December 2017

publication date

1 June 2003

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3 December 2017

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3 December 2017

volume

24

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3 December 2017

issue

2

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3 December 2017

page(s)

89-101

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A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3)

3 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.24.2.89.14001

A gene (SRPX) encoding a sushi-repeat-containing protein is deleted in patients with X-linked retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.24.2.89.14001

X-linked retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.24.2.89.14001

X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.24.2.89.14001

Phenotype-genotype correlations in X linked retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.24.2.89.14001

Genotype-phenotype correlation in X-linked retinitis pigmentosa 2 (RP2)

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.24.2.89.14001

X-linked Retinitis Pigmentosa Associated With a 2-Base Pair Insertion in Codon 99 of the RP3 Gene RPGR

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.24.2.89.14001

A new 2-base pair deletion in the RPGR gene in a black family with X-linked retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.24.2.89.14001

10.1076/OPGE.24.2.89.14001

21 January 2018

Identifiers

DOI

1 reference

3 December 2017

1 reference