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pro vyhledávání: '"Linda Cheung"'
Autor:
Duane Delimont, You Wei Peng, Mei Tian, Dominic Cosgrove, Weimin Wang, Linda Cheung, Marisa Zallocchi
Usher syndrome combines congenital hearing loss and retinitis pigmentosa (RP). Mutations in the whirlin gene (DFNB31/WHRN) cause a subtype of Usher syndrome (USH2D). Whirler mice have a defective whirlin gene. They have inner ear defects but usually
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::296b87695ad478a40eb8032a750720f5
https://europepmc.org/articles/PMC4408763/
https://europepmc.org/articles/PMC4408763/
Autor:
Kyriacos A. Mitrophanous, Michelle Kelleher, Yatish Lad, Linda Cheung, Weimin Wang, Vicky Scripps, Katie Binley, Marisa Zallocchi, You Wei Peng, Peter Widdowson, Dominic Cosgrove, S. Iqball, Scott Ellis, James Miskin, Julie Loader, Duane Delimont
Publikováno v:
PLoS ONE, Vol 9, Iss 4, p e94272 (2014)
PLoS ONE
PLoS ONE
Usher syndrome type 1B is a combined deaf-blindness condition caused by mutations in the MYO7A gene. Loss of functional myosin VIIa in the retinal pigment epithelia (RPE) and/or photoreceptors leads to blindness. We evaluated the impact of subretinal