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Mutation Spectrum of RB1 Gene in Unilateral Retinoblastoma Cases from Tunisia and Correlations with Clinical Features

Retinoblastoma, an embryonic neoplasm of retinal origin, is the most common primary intraocular malignancy in children. Somatic inactivation of both alleles of the RB1 tumor suppressor gene in a retinal progenitor cell through diverse mechanisms including genetic and epigenetic modifications, is the...

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Detalles Bibliográficos
Autores principales:	Ayari-Jeridi, Hajer, Moran, Kimberly, Chebbi, Amel, Bouguila, Hédi, Abbes, Imen, Charradi, Khaoula, Benammar-Elgaaïed, Amel, Ganguly, Arupa
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2015
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4300092/ https://www.ncbi.nlm.nih.gov/pubmed/25602518 http://dx.doi.org/10.1371/journal.pone.0116615

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