Dominantly inherited hyperinsulinism caused by a mutation in the sulfonylurea receptor type 1
J. Clin. Invest. Hanna Huopio, et al. 106:897 doi:10.1172/JCI9804 [Go to this article.]

Figure 2
Pedigree and haplotype analysis of a large pedigree carrying the SUR1 mutation E1506K. The order of markers of the haplotype is as follows: D11S1890, D11S921, D11S1888. The haplotypes are presented below each individual. The haplotype 3-4-4 associates with E1506K in all cases.