Rb1基因变异致视网膜母细胞瘤一例_Chinese Journal of Ocular Fundus Diseases

Authors：

孔京慧 , 章波 ,  宋银森

郑州大学附属儿童医院眼科河南省儿童医院郑州儿童医院河南省儿童遗传代谢性疾病重点实验室 450003;

Corresponding author：

宋银森, Email: df13607670608@163.com

Keywords：

基因，视网膜母细胞瘤; 病例报告

DOI：

10.3760/cma.j.issn.1005-1015.2020.02.015

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Citation： 孔京慧, 章波, 宋银森. Rb1基因变异致视网膜母细胞瘤一例. Chinese Journal of Ocular Fundus Diseases, 2020, 36(2): 150-150. doi: 10.3760/cma.j.issn.1005-1015.2020.02.015 Copy

1.	Ayari-Jeridi H, Moran K, Chebbi A, et al. Mutation spectrum of RB1 gene in unilateral retinoblastoma cases from Tunisia and correlations with clinical features[J/OL]. PLoS One, 2015, 10(1): 0116615[2015-01-20].https://doi.org/10.1371/journal.pone.0116615. DOI: 10.1371/journal.pone.0l16615.
2.	Abidi O, Knari S, Sefri H, et al. Mutational analysis of the RB1 gene in Moroccan patients with retinoblastoma[J]. Mol Vis, 2011, 12(17): 354l-3547.
3.	Dyson NJ. RBl: a prototype tumor suppressor and an enigma[J]. Genes Dev, 2016, 30(13): 1492-1502. DOI: 10.110l/gad.282145.116.

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Chinese Journal of Ocular Fundus Diseases

Rb1基因变异致视网膜母细胞瘤一例

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