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Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: Correlation of genotype and phenotype in 32 patients with hereditary hemochromatosis in China

Fig. 1

Representative pedigree analysis of four families. A Pedigree chart of family HH8. The patient (HH8) harbored homozygous variations of HJV p.C321X and HJV p.Q6H, which were inherited from their father and mother. B Pedigree chart of family HH10. The patient (HH10) harbored compound heterozygous variations of SLC40A1 p.Y333H and SUGP2 p.R639Q. C Pedigree chart of family HH13. The patient (HH13) harbored a single heterozygous variation of SLC40A1 p.Y333H, which was inherited from their mother. D Pedigree chart of family HH9. The patient (HH9) harbored compound heterozygous variations of SLC40A1 p.N144D and TFR2 p.R336H

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