(Q72874145)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7987385%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

title

Missense rhodopsin mutation in a family with recessive RP (English)

1 reference

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29 October 2019

author name string

Kumaramanickavel G

1

1 reference

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29 October 2019

Maw M

2

1 reference

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29 October 2019

Denton MJ

3

1 reference

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29 October 2019

John S

4

1 reference

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29 October 2019

Srikumari CR

5

1 reference

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29 October 2019

Orth U

6

1 reference

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29 October 2019

Oehlmann R

7

1 reference

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29 October 2019

Gal A

8

1 reference

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29 October 2019

publication date

1 September 1994

1 reference

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29 October 2019

1 reference

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29 October 2019

volume

8

1 reference

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29 October 2019

issue

1

1 reference

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29 October 2019

page(s)

10-11

1 reference

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https://scigraph.springernature.com/pub.10.1038/ng0994-10

29 October 2019

exact match

0 references

cites work

Rhodopsin mutation G90D and a molecular mechanism for congenital night blindness

1 reference

7 January 2021

Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Three cytoplasmic loops of rhodopsin interact with transducin

1 reference

7 January 2021

Identifiers

DOI

10.1038/NG0994-10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7987385%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

1 reference