FcγRIIIA Genotype in Plasma Cell Dyscrasias Is Associated with Clinical Progression, Bone Disease Extension and Immune Dysfunction.

Even after the stringent Bonferroni correction for multiple testing, the associations with bone disease, high-risk cytogenetics, and MAPK mutational status remained highly significant ( p adj < 0.001), supporting the notion that mutations are present throughout the natural history of plasma cell dyscrasias ( Table 4 ).

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