厚生労働科学研究費補助金(難治性疾患克服研究事業) 「Menkes 病・occipital horn 症候群の実態調査、早期診断基準確立、治療法開発に関する研究」 平成23年度 総括・分担研究報告書

厚生労働科学研究費補助金(難治性疾患克服研究事業) 「Menkes 病・occipital horn 症候群の実態調査、早期診断基準確立、治療法開発に関する研究」 平成23年度 総括・分担研究報告書(page 43/118)[厚生労働科学研究費補助金(難治性疾患克服研究事業) 「Menkes 病・occipital horn 症候群の実態調査、早期診断基準確立、治療法開発に関する研究」 平成23年度 総括・分担研究報告書]

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248 Current Drug Metabolism, 2012, Vol. 13, No. 3 Kodama et al.transporting ATPase gene in occipital horn syndrome and theblotchy mouse. Am. J. Hum. Genet., 1995, 56(3), 570-576.[12] Bull, P.C.; Thoma....

248 Current Drug Metabolism, 2012, Vol. 13, No. 3 Kodama et al.transporting ATPase gene in occipital horn syndrome and theblotchy mouse. Am. J. Hum. Genet., 1995, 56(3), 570-576.[12] Bull, P.C.; Thomas, G.R.; Rommens, J.M.; Forbes, J.R.; Cox, D.W.The Wilson disease gene is a putative copper transporting P-typeATPase similar to the Menkes gene. Nat. Genet., 1993, 5(4), 327-337.[13] Tanzi, R.E.; Petrukhin, K.; Chernov, I.; Pellequer, J.L.; Wasco, W.;Ross, B.; Romano, D.M.; Parano, E.; Pavone, L.; Brzustowicz,L.M.; Devoto, M.; Peppercorn, J.; Bush, A.I.; Sternlieb, I.; Pirastu,M.; Gusella, J.F.; Evgrafov, O.; Penchaszadeh, G.K.; Honig, B.;Edelman, I.S.; Soares, M.B.; Scheinberg, I.H.; Gilliam, T.C. TheWilson disease gene is a copper transporting ATPase with homologyto the Menkes disease gene. Nat. 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