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Genetic alterations of ALK in high-risk neuroblastoma patients: a SIOPEN study

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Background: In neuroblastoma (NB), the ALK receptor tyrosine kinase can be constitutively activated either through genomic amplification or activating point mutations. We studied ALK genetic alterations in high-risk NB patients to determine their frequency and prognostic impact.

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Neuroblastoma ALK Tumor Genomics Doenças Genéticas

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