(Q44393491)

2 December 2017

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

1 reference

2 December 2017

Zhao K

1

1 reference

2 December 2017

Xiong S

2

1 reference

2 December 2017

Wang L

3

1 reference

2 December 2017

Wang L

4

1 reference

2 December 2017

Cui Y

5

1 reference

2 December 2017

Wang Q

6

1 reference

2 December 2017

1 September 2001

1 reference

2 December 2017

8

1 reference

based on heuristic

inferred from page(s)

published in

Ophthalmic Genetics

1 reference

2 December 2017

22

1 reference

2 December 2017

3

1 reference

2 December 2017

155-162

1 reference

A point mutation of the rhodopsin gene in one form of retinitis pigmentosa

2 December 2017

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.22.3.155.2225

Isolation and nucleotide sequence of the gene encoding human rhodopsin

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.22.3.155.2225

Crystal structure of rhodopsin: A G protein-coupled receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.22.3.155.2225

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.22.3.155.2225

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.22.3.155.2225

Molecular genetics of retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.22.3.155.2225

A novel null mutation in the rhodopsin gene causing late onset autosomal dominant retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.22.3.155.2225

Mass spectrometric identification of phosphorylation sites in bleached bovine rhodopsin

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.22.3.155.2225

Rhodopsin trafficking and its role in retinal dystrophies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FOPGE.22.3.155.2225

10.1076/OPGE.22.3.155.2225

21 January 2018

Identifiers

DOI

1 reference

2 December 2017

1 reference