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IWWM-11 2022 | Novel FHL2 G226A mutation identified in familial Waldenström’s macroglobulinemia

Yike Wan, MD, Renji Hospital, Shanghai Jiao Tong University, Shanghai, China, briefly summarizes a study which used germline DNA exome sequencing to identify a novel FHL2 G226A mutation as a genetic variant that may contribute to familial cases of Waldenström’s macroglobulinemia (WM), and further highlights the importance of conducting genomic studies in this disease. This interview took place at the 11th International Workshop on Waldenström’s Macroglobulinemia (IWWM-11), held in Madrid, Spain.

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