(Q55670938)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8275096%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

title

A gene for Stargardt's disease (fundus flavimaculatus) maps to the short arm of chromosome 1 (English)

1 reference

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28 October 2019

2

1 reference

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28 October 2019

Jean-michel Rozet

4

1 reference

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28 October 2019

author name string

Kaplan J

1

1 reference

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28 October 2019

Larget-Piet D

3

1 reference

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28 October 2019

Dollfus H

5

1 reference

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28 October 2019

Dufier JL

6

1 reference

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28 October 2019

Odent S

7

1 reference

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28 October 2019

Postel-Vinay A

8

1 reference

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28 October 2019

Janin N

9

1 reference

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28 October 2019

Briard ML

10

1 reference

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28 October 2019

language of work or name

English

0 references

publication date

1 November 1993

1 reference

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28 October 2019

1 reference

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28 October 2019

volume

5

1 reference

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28 October 2019

page(s)

308-311

1 reference

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28 October 2019

issue

3

1 reference

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https://scigraph.springernature.com/pub.10.1038/ng1193-308

28 October 2019

exact match

0 references

cites work

Über familiäre, progressive Degeneration in der Maculagegend des Auges

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-308

Progressive cone-rod degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-308

Clinical and genetic heterogeneity in retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-308

7 January 2021

Fundus flavimaculatus. A clinical classification

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-308

7 January 2021

Fundus Flavimaculatus and Stargardt's Disease

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-308

7 January 2021

The dark choroid in posterior retinal dystrophies

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-308

7 January 2021

Butterfly-shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-308

7 January 2021

Infantile form of neuronal ceroid lipofuscinosis (CLN1) maps to the short arm of chromosome 1

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-308

7 January 2021

Batten disease (Spielmeyer-Vogt disease, juvenile onset neuronal ceroid-lipofuscinosis) gene (CLN3) maps to human chromosome 16.

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-308

7 January 2021

A second-generation linkage map of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-308

7 January 2021

Progressive cone dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-308

7 January 2021

The central and peripheral retina in macular degenerations. Involvement as reflected by the electroretinogram

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-308

7 January 2021

Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-308

7 January 2021

Retinal pigment epithelial abnormalities in fundus flavimaculatus: a light and electron microscopic study

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-308

7 January 2021

Evolution of the mammalian G protein alpha subunit multigene family

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-308

7 January 2021

On the molecular genetics of retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-308

7 January 2021

Identifiers

DOI

10.1038/NG1193-308

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8275096%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

28 October 2019

0 references

1 reference