(Q24309027)

6 December 2024

0 references

1 reference

GOA release 2020-03-11

visual perception

1 reference

GOA release 2020-03-11

1 reference

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9462750

6 December 2024

author name string

S. A. Hagstrom

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9462750

6 December 2024

M. A. North

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9462750

6 December 2024

P. L. Nishina

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9462750

6 December 2024

E. L. Berson

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9462750

6 December 2024

T. P. Dryja

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9462750

full work available at URL

6 December 2024

language of work or name

English

0 references

publication date

February 1998

0 references

http://www.nature.com/articles/ng0298-174

1 reference

http://www.nature.com/articles/ng0298-174.pdf

6 December 2024

1 reference

A candidate gene for the mouse mutation tubby

6 December 2024

0 references

18

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issue

2

0 references

page(s)

174-6

0 references

cites work

1 reference

Identification and characterization of the mouse obesity gene tubby: a member of a novel gene family

20 April 2017

1 reference

Molecular characterization of TUB, TULP1, and TULP2, members of the novel tubby gene family and their possible relation to ocular diseases

20 April 2017

1 reference

Mutations in the PDE6B gene in autosomal recessive retinitis pigmentosa

20 April 2017

1 reference

TULP1 mutation in two extended Dominican kindreds with autosomal recessive retinitis pigmentosa.

20 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0298-174

Ocular findings in patients with autosomal dominant retinitis pigmentosa and a rhodopsin gene defect (Pro-23-His).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0298-174

Ocular findings in patients with autosomal dominant retinitis pigmentosa and rhodopsin, proline-347-leucine

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0298-174

Fat (fat) and tubby (tub): two autosomal recessive mutations causing obesity syndromes in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0298-174

7 January 2021

Cochlear and retinal degeneration in the tubby mouse

1 reference

https://api.crossref.org/works/10.1038%2FNG0298-174

7 January 2021

A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1038%2FNG0298-174

7 January 2021

Missense rhodopsin mutation in a family with recessive RP

1 reference

https://api.crossref.org/works/10.1038%2FNG0298-174

7 January 2021

Mutation spectrum of the gene encoding the beta subunit of rod phosphodiesterase among patients with autosomal recessive retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1038%2FNG0298-174

7 January 2021

Homozygous tandem duplication within the gene encoding the beta-subunit of rod phosphodiesterase as a cause for autosomal recessive retinitis pigmentosa.

1 reference

https://api.crossref.org/works/10.1038%2FNG0298-174

7 January 2021

Autosomal recessive retinitis pigmentosa caused by mutations in the alpha subunit of rod cGMP phosphodiesterase

1 reference

https://api.crossref.org/works/10.1038%2FNG0298-174

7 January 2021

Mutations in the gene encoding the alpha subunit of the rod cGMP-gated channel in autosomal recessive retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1038%2FNG0298-174

7 January 2021

Mutation of the gene encoding cellular retinaldehyde-binding protein in autosomal recessive retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1038%2FNG0298-174

7 January 2021

Mutations in RPE65 cause autosomal recessive childhood–onset severe retinal dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0298-174

7 January 2021

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

1 reference

https://api.crossref.org/works/10.1038%2FNG0298-174

7 January 2021

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

1 reference

https://api.crossref.org/works/10.1038%2FNG0298-174

7 January 2021

Human Molecular Genetics

6

31

401

JA Knowles

1994

1 reference

Electroretinographic testing as an aid in detection of carriers of X-chromosome-linked retinitis pigmentosa

6 December 2024

22

1 reference