(Q84424536)

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5 February 2020

title

Linkage analysis and mutation screening of the rhodopsin gene in a Chinese Bai family with autosomal dominant retinitis pigmentosa (English)

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5 February 2020

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2

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5 February 2020

author name string

Haike Guo

1

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5 February 2020

Qianli Meng

3

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5 February 2020

Hongyang Zhang

4

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5 February 2020

Haiying Jin

5

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5 February 2020

Yanlei Chen

6

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5 February 2020

publication date

17 June 2010

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20555336%20AND%20SRC:MED&resulttype=core&format=json

Journal of Human Genetics

5 February 2020

published in

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5 February 2020

volume

55

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5 February 2020

issue

9

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5 February 2020

page(s)

571-576

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https://scigraph.springernature.com/pub.10.1038/jhg.2010.68

5 February 2020

exact match

0 references

cites work

Prevalence of retinitis pigmentosa in urban and rural adult Chinese: The Beijing Eye Study.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.68

7 January 2021

https://api.crossref.org/works/10.1038%2FJHG.2010.68

1 reference

7 January 2021

Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.68

7 January 2021

Novel rhodopsin mutation in a Chinese family with autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.68

7 January 2021

Mechanisms of cell death in rhodopsin retinitis pigmentosa: implications for therapy

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.68

7 January 2021

Mechanisms of apoptosis in retinitis pigmentosa.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.68

7 January 2021

Point mutations of rhodopsin gene found in Japanese families with autosomal dominant retinitis pigmentosa (ADRP)

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.68

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.68

7 January 2021

Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.68

7 January 2021

Further screening of the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.68

7 January 2021

Mutation analysis of codons 345 and 347 of rhodopsin gene in Indian retinitis pigmentosa patients

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.68

7 January 2021

Diagnosis of autosomal dominant retinitis pigmentosa by linkage-based exclusion screening with multiple locus-specific microsatellite markers

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.68

7 January 2021

Low frequency of rhodopsin mutations in South African patients with autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.68

7 January 2021

Molecular genetic study of autosomal dominant retinitis pigmentosa in Lithuanian patients

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.68

7 January 2021

Rhodopsin mutations in Chinese patients with retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.68

7 January 2021

Mechanisms of rhodopsin inactivation in vivo as revealed by a COOH-terminal truncation mutant.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.68

7 January 2021

Rapid and reproducible deactivation of rhodopsin requires multiple phosphorylation sites

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.68

7 January 2021

Mutations and common polymorphisms in ADAMTS13 gene responsible for von Willebrand factor-cleaving protease activity

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.68

7 January 2021

Modulation of ADAMTS13 secretion and specific activity by a combination of common amino acid polymorphisms and a missense mutation

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.68

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.68

7 January 2021

Novel PRPF31 and PRPH2 mutations and co-occurrence of PRPF31 and RHO mutations in Chinese patients with retinitis pigmentosa.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.68

7 January 2021

Identifiers

DOI

10.1038/JHG.2010.68

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20555336%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

1 reference