(Q28250918)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9326927%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

title

Mutations in RPE65 cause Leber's congenital amaurosis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9326927%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

0 references

4

1 reference

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6 November 2019

author name string

Marlhens F

1

1 reference

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6 November 2019

Bareil C

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9326927%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Griffoin JM

3

1 reference

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6 November 2019

Amalric P

5

1 reference

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6 November 2019

Eliaou C

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9326927%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Liu SY

7

1 reference

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6 November 2019

Harris E

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9326927%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Redmond TM

9

1 reference

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6 November 2019

Arnaud B

10

1 reference

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6 November 2019

Claustres M

11

1 reference

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6 November 2019

Hamel CP

12

1 reference

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6 November 2019

language of work or name

English

0 references

publication date

1 October 1997

1 reference

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6 November 2019

1 reference

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6 November 2019

volume

17

1 reference

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6 November 2019

page(s)

139-141

1 reference

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6 November 2019

issue

2

1 reference

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https://scigraph.springernature.com/pub.10.1038/ng1097-139

6 November 2019

exact match

0 references

cites work

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

1 reference

https://api.crossref.org/works/10.1038/NG1097-139

The gene for the retinal pigment epithelium-specific protein RPE65 is localized to human 1p31 and mouse 3

20 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG1097-139

A developmentally regulated microsomal protein specific for the pigment epithelium of the vertebrate retina

20 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-139

7 January 2021

Inherited retinal degeneration: exceptional genetic and clinical heterogeneity

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-139

7 January 2021

Inherited Retinal Dystrophy: Primary Defect in Pigment Epithelium Determined with Experimental Rat Chimeras

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-139

7 January 2021

A gene for Leber's congenital amaurosis maps to chromosome 17p

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-139

7 January 2021

Classification of congenital and early onset retinitis pigmentosa.

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-139

7 January 2021

Phenotype correction in retinal pigment epithelium in murine mucopolysaccharidosis VII by adenovirus-mediated gene transfer

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-139

7 January 2021

Identifiers

DOI

10.1038/NG1097-139

2 references

Consolidated OpenCitations Corpus – April 2017

890815

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9326927%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

890815

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

890815