Homozygous tandem duplication within the gene encoding the β-subunit of rod phosphodiesterase as a cause for autosomal recessive retinitis pigmentosa-Reference-Cited by-同舟云学术

Homozygous tandem duplication within the gene encoding the β-subunit of rod phosphodiesterase as a cause for autosomal recessive retinitis pigmentosa

Published:1995 Issue:3 Volume:5 Page:228-234
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Bayés Mònica,Giordano Mara,Balcells Susana,Grinberg Daniel,Vilageliu Llusïsa,Martínez Immaculada,Ayuso Carmen,Benítez Javier,Ramos-Arroyo María A.,Chivelet Pilar,Solans Teresa,Valverde Diana,Amselem Serge,Goossens Michel,Baiget Montserrat,Gonzàlez-Duarte Roser,Besmond Claude

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference29 articles.

1. Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19

2. Detection by PCR of the VNTR polymorphism at D4S95

3. Nonsense mutations in the human beta-globin gene affect mRNA metabolism.

4. Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8

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