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Autor:
I. E. Guryanova, A. V. Liubushkin, O. O. Makarevich, D. Yu. Litvinova, V. R. Vertеlko, A. V. Valochnik, E. A. Polyakova, A. A. Migas, N. E. Konoplya
Publikováno v:
Pediatric Hematology/Oncology and Immunopathology. 21:78-88
Retinoblastoma is an aggressive eye tumor originating from maturing cone precursors in the developing retina and most commonly seen in childhood. In 98 % of patients, retinoblastoma is caused by bi-allelic inactivation of the RB1 tumor suppressor gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80adecc93e93616d1ee9085fafa9963a
https://doi.org/10.24287/1726-1708-2022-21-2-78-88
https://doi.org/10.24287/1726-1708-2022-21-2-78-88
