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Year Number of Results
2011 1
2012 1
2015 4
2016 4
2019 3
2020 4
2021 6
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Page 1
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: miyagawa 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
[Herpes simplex virus].
Shibata M, Miyagawa K, Harada M. Shibata M, et al. Among authors: miyagawa k. Nihon Rinsho. 2015 Dec;73 Suppl 9:650-3. Nihon Rinsho. 2015. PMID: 26846015 Japanese. No abstract available.
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