“…Like the latter allele, they were included in the class II-deduced haplotype DQA1*050101-DQB1*0201 (Table 2). DRB1*1111 was first described in a Caucasian individual demonstrating two nucleotide mutations at codon 71 (AGG Ͼ GAG) with regard to DRB1*110101 [22]. We have analyzed the complete coding sequence of DRB1*1111 allele in the cord blood unit CTM-3095924.…”