The p.Arg86Gln change in GARP2 (glutamic acid-rich protein-2) is a common West African-related polymorphism

Author:

Gibriel Abdullah A.Y.,Tate Rothwelle J.,Yu Yongbin,Rawson-Lax Emma,Hammer Harold M.,Tettey Justice N.A.,Pyne Nigel J.,Converse Carolyn A.

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference16 articles.

1. cDNA, gene structure, and chromosomal localization of human GAR1 (CNCG3L), a homolog of the third subunit of bovine photoreceptor cGMP-gated channel;Ardell;Genomics,1995

2. Segregation of a mutation in CNGB1 encoding the beta-subunit of the rod cGMP-gated channel in a family with autosomal recessive retinitis pigmentosa;Bareil;Hum. Genet.,2001

3. Evaluation of the GARP portion of the human rod cGMP-gated channel β subunit gene in patients with autosomal recessive retinitis pigmentosa;Bharadwaj;Invest. Ophthalmol. Vis. Sci.,1999

4. Prediction of human mRNA donor and acceptor sites from the DNA sequence;Brunak;J. Mol. Biol.,1991

5. Gibriel AAY. Visual transduction proteins and their involvement in retinal disease, PhD Thesis, 2008, Glasgow, UK, University of Strathclyde.

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