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Paper Details

Exome sequencing reveals recurrent germ line variants in patients with familial Waldenström macroglobulinemia.
Blood
14
2016
B, B-cell lymphoproliferative disorders, HCLS1, HCLS1(, HCLS1(g496a), LAPTM5, LAPTM5(, WM, Waldenstrm macroglobulinemia, familial WM, familial Waldenstrm macroglobulinemia, germ line, germ line DNA, patients, predisposition alleles, tumor, tumor clone
Author NameAffiliation
Matthew L FreedmanDana-Farber Cancer Institute, Harvard Medical School
Matthew L FreedmanDana-Farber Cancer Institute, Harvard Medical School
Eliezer M Van AllenDana-Farber Cancer Institute, Harvard Medical School
Eliezer M Van AllenDana-Farber Cancer Institute, Harvard Medical School
Winston HideHarvard School of Public Health
Winston HideHarvard School of Public Health
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Release 1.2