Myotonic dystrophy type 2 (DM2) is definitely a dominantly inherited autosomal disease with multi-systemic Rivaroxaban Diol medical features and it is caused by expansion of a CCTG tetranucleotide repeat in the 1st intron of the zinc finger protein 9 (ZNF9) gene in 3q21. at fluorescence and transmission electron microscopy by using a panel of antibodies… Continue reading Myotonic dystrophy type 2 (DM2) is definitely a dominantly inherited autosomal