Zobrazeno 1 - 3
of 3
pro vyhledávání: '"11-cis retinol dehydrogenase mutation"'
Autor:
Ethan K. Sobol, Avnish Deobhakta, Carl S. Wilkins, Jasmine H. Francis, Toco Y.P. Chui, Alfredo Dubra, Davis B. Zhou, Maria V. Castanos, Gareth M.C. Lema, Richard B. Rosen, Justin V. Migacz
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 22, Iss , Pp 101090- (2021)
Purpose: Fundus albipunctatus is an inherited cause of congenital stationary night blindness. The objective of this report is to describe structural changes occurring in a macular phenotype of a novel RDH5 mutation producing fundus albipunctatus usin
Externí odkaz:
https://doaj.org/article/7f995208ef2f476c9610065978c12550
Autor:
Alfredo Dubra, Gareth M.C. Lema, Toco Yuen Ping Chui, Carl S. Wilkins, Davis B. Zhou, Justin V Migacz, Avnish Deobhakta, Ethan K. Sobol, Jasmine H. Francis, Richard B Rosen, Maria V. Castanos
Publikováno v:
American Journal of Ophthalmology Case Reports
American Journal of Ophthalmology Case Reports, Vol 22, Iss, Pp 101090-(2021)
American Journal of Ophthalmology Case Reports, Vol 22, Iss, Pp 101090-(2021)
Purpose Fundus albipunctatus is an inherited cause of congenital stationary night blindness. The objective of this report is to describe structural changes occurring in a macular phenotype of a novel RDH5 mutation producing fundus albipunctatus using
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ae5d9ac064c9de4b7a6e95a8debe4bc
http://europepmc.org/articles/PMC8082516
http://europepmc.org/articles/PMC8082516
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