https://www.selleckchem.com/pr....oducts/gsk2643943a.h
Myotonic dystrophy type 2 (DM2) is caused by a CCTG repeat expansion in intron 1 of the CCHC-Type Zinc Finger Nucleic Acid Binding Protein (CNBP) gene. Previous studies indicated that this repeat expansion originates from separate founders. This study was set out to determine whether or not patients with DM2 originating from European and non-European countries carry the previously described European founder haplotypes. Haplotype analysis was performed in 59 DM2 patients from 29 unrelated families. Twenty-three families were from Eur
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