Next generation sequencing of RB1gene for the molecular diagnosis of ethnic minority with retinoblastoma in Yunnan

BACKGROUND: Retinoblastoma is a rare intraocular malignancy and typically initiated by inactivating biallelic mutations of RB1 gene. Each year, ~ 8000 children worldwide are diagnosed for retinoblastoma. In high-income countries, patient survival is over 95% while low-income countries is ~ 30%.If di...

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Detalles Bibliográficos
Autores principales: Zhang, Zhen, Xiao, Yi-shuang, Shen, Ru, Jiang, Hong-chao, Tan, Li, Li, Ren-qiu, Yang, Xiao-hong, Gu, Huai-yu, He, Wen-Ji, Ma, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7682003/
https://www.ncbi.nlm.nih.gov/pubmed/33225895
http://dx.doi.org/10.1186/s12881-020-01150-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7682003/
https://www.ncbi.nlm.nih.gov/pubmed/33225895
http://dx.doi.org/10.1186/s12881-020-01150-7

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