(Q28244150)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8019570%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

title

Mutations in the human peripherin/RDS gene associated with autosomal dominant retinitis pigmentosa (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8019570%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

1 reference

8

1 reference

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23 October 2019

author name string

Grüning G

1

1 reference

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23 October 2019

Millan JM

2

1 reference

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23 October 2019

Meins M

3

1 reference

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23 October 2019

Beneyto M

4

1 reference

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23 October 2019

Caballero M

5

1 reference

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23 October 2019

Apfelstedt-Sylla E

6

1 reference

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23 October 2019

Bosch R

7

1 reference

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23 October 2019

Prieto F

9

1 reference

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23 October 2019

Gal A

10

1 reference

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23 October 2019

language of work or name

English

0 references

publication date

1 January 1994

1 reference

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23 October 2019

1 reference

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23 October 2019

volume

3

1 reference

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23 October 2019

issue

3

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23 October 2019

page(s)

321-323

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8019570%20AND%20SRC:MED&resulttype=core&format=json

Molecular Analysis and Genetic Mapping of the Rhodopsin Gene in Families with Autosomal Dominant Retinitis Pigmentosa

23 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030326

7 January 2021

A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030326

7 January 2021

Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030326

7 January 2021

A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the fovea

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030326

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/10.1002%2FHUMU.1380030326

7 January 2021

The human retinal degeneration slow (RDS) gene: Chromosome assignment and structure of the mRNA

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030326

7 January 2021

A medley of retinal dystrophies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030326

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380030326

7 January 2021

Identifiers

DOI

10.1002/HUMU.1380030326

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8019570%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

1 reference