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[文献書誌] 佐藤浩: "遺伝性黄疸-Crigler-Najjar症候群とGilbert症候群の遺伝子解析-" Porphyrins. 5. 177-184 (1996)
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[文献書誌] Kamisako,T.: "Mutiplicity of mutation in UDP-glucuronosylktransferase 1^*1 gene in Gilbert's syndrome." Int.Hepatol.Commun.6. 249-252 (1997)
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[文献書誌] 添田陽子: "Gilbert症候群患者におけるビリルビンUDP-グルクロン酸転移酵素遺伝子のTATA boxとコード領域の解析." 滋賀医科大学雑誌. 12. 61-70 (1997)
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[文献書誌] 足立幸彦: "体質性黄疸の分子生物学的研究の進歩" 日本内科学雑誌. 86. 1467-1469 (1997)
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[文献書誌] Maruo,Y.: "Gilbert's syndrome due to a homozygous mis-sense mutation (Tyr486Asp) of bilirubin UDP-glycuronosyltransferase gene." J.Pediat.(in press).
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[文献書誌] Yamamoto,K.: "Contribution of two missense mutations (G71R and Y486D) of the UGT1A1 gene to phenotypes of Gilbert's syndrome and Crigler-Najjar syndrome type II" Biochim.Biophys.Acta. (in press).
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[文献書誌] Yamamoto,K.: "Mutation analysis of seven patlents with Crigler-Najjar syndrome type II" J.Hum.Genet.(in press).
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[文献書誌] Ueyama,H.: "Analysis of the promoter of bilirubin UDP-glyucuronosyl transferase gene (UGT1^*1) in relevance to Gilbert's syndrome." Hepatol.Res.(in press).