Zobrazeno 1 - 2
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pro vyhledávání: '"J W B, Bainbridge"'
Autor:
A, Georgiadis, Y, Duran, J, Ribeiro, L, Abelleira-Hervas, S J, Robbie, B, Sünkel-Laing, S, Fourali, A, Gonzalez-Cordero, E, Cristante, M, Michaelides, J W B, Bainbridge, A J, Smith, R R, Ali
Publikováno v:
Gene Therapy
Leber congenital amaurosis is a group of inherited retinal dystrophies that cause severe sight impairment in childhood; RPE65-deficiency causes impaired rod photoreceptor function from birth and progressive impairment of cone photoreceptor function a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::11efeb72a0ca4d7255b748b4cf57010b
https://pubmed.ncbi.nlm.nih.gov/30046128
https://pubmed.ncbi.nlm.nih.gov/30046128
Autor:
A, Georgiadis, Y, Duran, J, Ribeiro, L, Abelleira-Hervas, S J, Robbie, B, Sünkel-Laing, S, Fourali, A, Gonzalez-Cordero, E, Cristante, M, Michaelides, J W B, Bainbridge, A J, Smith, R R, Ali
Publikováno v:
Gene Therapy
Leber congenital amaurosis is a group of inherited retinal dystrophies that cause severe sight impairment in childhood; RPE65-deficiency causes impaired rod photoreceptor function from birth and progressive impairment of cone photoreceptor function a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a401d5be536850967d31f0d33ab8aba
https://doi.org/10.1038/s41434-018-0031-x
https://doi.org/10.1038/s41434-018-0031-x