Erratum to: Imprinting disorders: A group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci (Clin Epigenetics, (2015), 7, (123), 10.1186/s13148-015-0143-8)

Abstract

Unfortunately, after publication of the original version of this article [1], it was noticed that there were some errors in Fig. 3 and Fig. 4: • In Fig. 3, the methylation of H19/IGF2:IG-DMR hypomethylation is not correctly illustrated: the lolly pops should be empty (=unmethylated). • In Fig. 4, the methylation of both H19/IGF2:IGDMR hypermethylation and KCNQ1OT1:TSS-DMR hypomethylation are not correctly illustrated: in case of the H19/IGF2:IG-DMR hypermethylation the lolly pops should be filled (=methylated), and for the KCNQ1OT1:TSS-DMR, they should be empty (=unmethylated). The corrected Fig. 3 and Fig. 4 have been included in this erratum.