USH2A Mutation analysis in 70 Dutch families with Usher syndrome type II-Reference-Cited by-同舟云学术

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USH2A Mutation analysis in 70 Dutch families with Usher syndrome type II

Published:2004 Issue:2 Volume:24 Page:185-185
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Pennings Ronald J.E.,te Brinke Heleen,Weston Michael D.,Claassen Annemarie,Orten Dana J.,Weekamp Henri�tte,van Aarem Annelies,Huygen Patrick L.M.,Deutman August F.,Hoefsloot Lies H.,Cremers Frans P.M.,Cremers Cor W.R.J.,Kimberling William J.,Kremer Hannie

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Cited by 45 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. Usher Syndrome Type 2 in An Iranian Family: A Novel Founder Variation in The USH2A Gene;CELL J;2024

2. Genetic profile of syndromic retinitis pigmentosa in Portugal;Graefe's Archive for Clinical and Experimental Ophthalmology;2024-01-08

3. USH2A variants causing retinitis pigmentosa or Usher syndrome provoke differential retinal phenotypes in disease-specific organoids;Human Genetics and Genomics Advances;2023-10

4. Genetic Characteristics and Variation Spectrum of USH2A-Related Retinitis Pigmentosa and Usher Syndrome;Frontiers in Genetics;2022-08-30

5. Early audiological phenotype in patients with mutations in the USH2A gene;International Journal of Pediatric Otorhinolaryngology;2022-06

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