Genetik des Usher-Syndroms
Author:
Publisher
Springer Science and Business Media LLC
Subject
Ophthalmology
Link
http://link.springer.com/content/pdf/10.1007/s00347-008-1887-8.pdf
Reference44 articles.
1. Adato A, Kalinski H, Weil D et al (1999) Possible interaction between USH1B and USH3 gene products as implied by apparent digenic deafness inheritance. Am J Hum Genet 65:261–265
2. Adato A, Vreugde S, Joensuu T et al (2002) USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses. Eur J Hum Genet 10:339–350
3. Ahmed ZM, Riazuddin S, Bernstein Sl et al (2001) Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F. Am J Hum Genet 69:25–34
4. Ahmed ZM, Riazuddin S, Khan SN et al (2009) USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23. Clin Genet 75:86–91
5. Alagramam KN, Yuan H, Kuehn MH et al (2001) Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F. Hum Mol Genet 10:1709–1718
Cited by 2 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. Psychological Stress in People with Dual Sensory Impairment through Usher Syndrome Type II;Journal of Visual Impairment & Blindness;2015-05
2. The molecular basis of human retinal and vitreoretinal diseases;Progress in Retinal and Eye Research;2010-09
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