Next-generation sequencing-based method shows increased mutation detection sensitivity in an Indian retinoblastoma cohort

PURPOSE: Retinoblastoma (Rb) is the most common primary intraocular cancer of childhood and one of the major causes of blindness in children. India has the highest number of patients with Rb in the world. Mutations in the RB1 gene are the primary cause of Rb, and heterogeneous mutations are distribu...

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Detalhes bibliográficos
Publicado no:Mol Vis
Main Authors: Singh, Jaya, Mishra, Avshesh, Pandian, Arunachalam Jayamuruga, Mallipatna, Ashwin C., Khetan, Vikas, Sripriya, S., Kapoor, Suman, Agarwal, Smita, Sankaran, Satish, Katragadda, Shanmukh, Veeramachaneni, Vamsi, Hariharan, Ramesh, Subramanian, Kalyanasundaram, Mannan, Ashraf U.
Formato: Artigo
Idioma:Inglês
Publicado em: Molecular Vision 2016
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4985049/
https://ncbi.nlm.nih.gov/pubmed/27582626
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