TMPRSS3 and nodular sclerosis classical Hodgkin lymphoma: (ii) AR NSHL displays pronounced locus heterogeneity with 85 genes/loci listed in OMIM (http://omim.org/phenotypicSeries/PS220290), (iii) the TMPRSS3 gene mutations are a relatively rare cause of NSHL in Caucasians4, with so far no reports from Polish population.