Prevalence of 2314delG mutation in Spanish patients with Usher syndrome type II (USH2)-Reference-Cited by-同舟云学术

Prevalence of 2314delG mutation in Spanish patients with Usher syndrome type II (USH2)

Published:2000-01 Issue:2 Volume:21 Page:123-128
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Beneyto Magdalena,Cuevas José M.,Millán José M.,Espinós Carmen,Mateu Emilia,González-Cabo Pilar,Baiget Montserrat,Doménech Montserrat,Bernal Sara,Ayuso Carmen,García-Sandoval Blanca,Trujillo Ma José,Borrego Salud,Antiñolo Guillermo,Carballo Miguel,Nájera Carmen

Publisher

Swets & Zeitlinger Publishers

Subject

Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health

Link

http://www.tandfonline.com/doi/pdf/10.1076/1381-6810(200006)2121-8FT123

Reference11 articles.

1. Clinical diagnosis of the Usher syndromes

2. Localization of Usher syndrome type II to chromosome 1q

Cited by 7 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. Antisense Oligonucleotides for the Treatment of Inner Ear Dysfunction;Neurotherapeutics;2019-04

2. Targeted next generation sequencing in Italian patients with Usher syndrome: phenotype-genotype correlations;Scientific Reports;2017-11-15

3. Frecuencia de mutaciones en el gen de la usherina (USH2A) en 26 individuos colombianos con síndrome de Usher, tipo II;Biomédica;2011-04-16

4. Mutation analysis in the long isoform of USH2A in American patients with Usher Syndrome type II;Journal of Human Genetics;2009-10-30

5. Detection of Genomic Variation by Selection of a 9 Mb DNA Region and High Throughput Sequencing;PLoS ONE;2009-08-17