Publication | Open Access
Exome Sequencing Identifies Autosomal-Dominant SRP72 Mutations Associated with Familial Aplasia and Myelodysplasia
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2012
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Somatic VariantFamilial AplasiaMendelian DisorderGenetic DisorderMedicineGeneticsMolecular GeneticsDisease Gene IdentificationMolecular DiagnosticsCell BiologyMyeloid Neoplasia
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