Type 4B hereditary hemochromatosis due to heterozygous p.D157A mutation in SLC40A1 complicated with hypopituitarism.
Honma Y, Karasuyama T, Kumamoto K, Shimajiri S, Toki Y, Tatsumi Y, Sumida K, Koikawa K, Morino K, Oe S, Miyagawa K, Yamasaki M, Shibata M, Abe S, Ikuta K, Hayashi H, Harada M.
Honma Y, et al. Among authors: sumida k.
Med Mol Morphol. 2021 Mar;54(1):60-67. doi: 10.1007/s00795-020-00259-1. Epub 2020 Jun 30.
Med Mol Morphol. 2021.
PMID: 32607777