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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4985049/
https://www.ncbi.nlm.nih.gov/pubmed/27582626

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