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bibliographicCitation Zemet R, Du H, Gambin T, Lupski JR, Liu P, Stankiewicz P. SNV/indel hypermutator phenotype in biallelic RAD51C variant: Fanconi anemia. Hum Genet. 2023 Jun;142(6):721–33. doi: 10.1007/s00439-023-02550-4. PMID: 37031326.
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title SNV/indel hypermutator phenotype in biallelic RAD51C variant: Fanconi anemia
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