(Q43671138)

25 November 2017

title

Screening for CRX gene mutations in Chinese patients with Leber congenital amaurosis and mutational phenotype (English)

1 reference

Leber congenital amaurosis

25 November 2017

0 references

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Zhang Q

1

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25 November 2017

Li S

2

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25 November 2017

Guo X

3

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25 November 2017

Guo L

4

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25 November 2017

Xiao X

5

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25 November 2017

Jia X

6

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25 November 2017

Kuang Z

7

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25 November 2017

publication date

1 June 2001

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25 November 2017

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25 November 2017

volume

22

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25 November 2017

issue

2

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25 November 2017

page(s)

89-96

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

25 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.22.2.89.2227

Mutations in RPE65 cause Leber's congenital amaurosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.22.2.89.2227

De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.22.2.89.2227

Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.22.2.89.2227

A novel locus for Leber congenital amaurosis on chromosome 14q24.

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.22.2.89.2227

A novel locus for Leber congenital amaurosis maps to chromosome 6q

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.22.2.89.2227

Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor function

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.22.2.89.2227

Mutation analysis of 3 genes in patients with Leber congenital amaurosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.22.2.89.2227

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.22.2.89.2227

10.1076/OPGE.22.2.89.2227

21 January 2018

Identifiers

DOI

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25 November 2017

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