A New Locus for Autosomal Recessive Retinitis Pigmentosa (RP19) Maps to 1p13

A New Locus for Autosomal Recessive Retinitis Pigmentosa (RP19) Maps to 1p13–1p21

Published:1997-02 Issue:1 Volume:40 Page:142-146
ISSN:0888-7543
Container-title:Genomics
language:en
Short-container-title:Genomics

Author:

Martı́nez-Mir Amalia,Bayés Mònica,Vilageliu Lluı̈sa,Grinberg Daniel,Ayuso Carmen,Rı́o Teresa del,Garcı́a-Sandoval Blanca,Bussaglia Elena,Baiget Montserrat,Gonzàlez-Duarte Roser,Balcells Susana

Publisher

Elsevier BV

Subject

Genetics

Reference32 articles.

1. A YAC contig encompassing the recessive Stargardt disease gene (STGD) on chromosome 1p;Anderson;Am. J. Hum. Genet.,1995

2. Retinitis pigmentosa in Spain;Ayuso;Clin. Genet.,1995

3. Homozygous tandem duplication within the gene encoding the beta-subunit of rod phosphodiesterase as a cause for autosomal recessive retinitis pigmentosa;Bayés;Hum. Mutat.,1995

4. Chromosomal localization of genes encoding guanine nucleotide-binding protein subunits in mouse and human;Blatt;Proc. Natl. Acad. Sci. USA,1988

5. Integrated human genome-wide maps constructed using the CEPH reference panel;Buetow;Nature Genet.,1994

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