A novel locus for autosomal dominant cone-rod dystrophy maps to chromosome 10q-Reference-Cited by-同舟云学术

A novel locus for autosomal dominant cone-rod dystrophy maps to chromosome 10q

Published:2012-08-29 Issue:3 Volume:21 Page:338-342
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Kamenarova Kunka,Cherninkova Sylvia,Romero Durán Margarita,Prescott DeQuincy,Valdés Sánchez Maria Lourdes,Mitev Vanio,Kremensky Ivo,Kaneva Radka,Bhattacharya Shomi S,Tournev Ivailo,Chakarova Christina

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/ejhg2012158.pdf

Reference15 articles.

1. Moore AT : Cone and cone-rod dystrophies. J Med Genet 1992; 29: 289–290.

2. Michaelides M, Hardcastle AJ, Hunt DM, Moore AT : Progressive cone and cone-rod dystrophies: phenotypes and underlying molecular genetic basis. Surv Ophthalmol 2006; 51: 232–258.

3. Morar B, Gresham D, Angelicheva D et al. Mutation history of the roma/gypsies. Am J Hum Genet 2004; 75: 596–609.

4. Kalaydjieva L, Morar B, Chaix R, Tang H : A newly discovered founder population: the Roma/Gypsies. Bioessays 2005; 27: 1084–1094.

5. Lindner T, Hoffmann K : easyLINKAGE: a PERL script for easy and automated two-/multi-point linkage analyses. Bioinformatics 2005; 21: 405–407.

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Novel eye genes systematically discovered through an integrated analysis of mouse transcriptomes and phenome;Computational and Structural Biotechnology Journal;2020

2. An atlas of gene expression and gene co-regulation in the human retina;Nucleic Acids Research;2016-05-27

3. A novel CRX mutation by whole-exome sequencing in an autosomal dominant cone-rod dystrophy pedigree;INT J OPHTHALMOL-CHI;2015

4. Clinical Characteristics and Current Therapies for Inherited Retinal Degenerations;Cold Spring Harbor Perspectives in Medicine;2014-10-16