Optimization of Capillary-Based Western Blotting for MYO7A
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-031-27681-1_19
Reference14 articles.
1. Ouyang XM, Yan D, Du LL, Hejtmancik JF, Jacobson SG, Nance WE, et al. Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population. Hum Genet. 2005;116(4):292–9. https://doi.org/10.1007/s00439-004-1227-2.
2. Jaijo T, Aller E, Beneyto M, Najera C, Graziano C, Turchetti D, et al. MYO7A mutation screening in Usher syndrome type I patients from diverse origins. J Med Genet. 2007;44(3):e71. https://doi.org/10.1136/jmg.2006.045377.
3. Stabej PL, Saihan Z, Rangesh N, Steele-Stallard HB, Ambrose J, Coffey A, et al. Comprehensive sequence analysis of nine Usher syndrome genes in the UK National Collaborative Usher Study. J Med Genet. 2012;49(1):27–36. https://doi.org/10.1136/jmedgenet-2011-100468.
4. Jacobson SG, Cideciyan AV, Aleman TS, Sumaroka A, Roman AJ, Gardner LM, et al. Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism. Hum Mol Genet. 2008;17(15):2405–15. https://doi.org/10.1093/hmg/ddn140.
5. Jacobson SG, Aleman TS, Sumaroka A, Cideciyan AV, Roman AJ, Windsor EA, et al. Disease boundaries in the retina of patients with usher syndrome caused by MYO7A gene mutations. Invest Ophthalmol Vis Sci. 2009;50(4):1886–94. https://doi.org/10.1167/iovs.08-3122.
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