A new locus (RP31) for autosomal dominant retinitis pigmentosa maps to chromosome 9p-Reference-Cited by-同舟云学术

A new locus (RP31) for autosomal dominant retinitis pigmentosa maps to chromosome 9p

Published:2005-09-28 Issue:3-4 Volume:118 Page:501-503
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Papaioannou Myrto,Chakarova Christina F.,Prescott De Quincy C.,Waseem Naushin,Theis Thorsten,Lopez Irma,Gill Bhavdip,Koenekoop Robert K.,Bhattacharya Shomi S.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-005-0063-3.pdf

Reference5 articles.

1. Berson EL (1993) Retinitis pigmentosa. The Friedenwald lecture. Invest Ophthalmol Vis Sci 34:1659–1676

2. Bundey S, Crews SJ (1984) A study of retinitis pigmentosa in the city of Birmingham-I. Prevalence. J Med Genet 21:417–420

3. Dryja TP, Li T (1995) Molecular genetics of retinitis pigmentosa. Hum Mol Genet 4:1739–1743

4. Himms MM, Daiger SP, Inglehearn CF (2003) Retinitis pigmentosa: genes, proteins and prospects. Dev Ophthalmol 37:109–125

5. Inglehearn CF, Tarttelin EE, Plant C, Peacock RE, al-Maghtheh M, Vithana E, Bird AC, Bhattacharya SS (1998) A linkage survey of 20 dominant retinitis pigmentosa families: frequencies of the nine known loci and evidence for further heterogeneity. J Med Genet 35:1–5

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