Homozygous mutation Arg_<768> Trp in the ABC-transporter encoding gene MRP2/cMOAT/ABCC2 causes Dubin-Johnson syndrome in a Caucasian patient

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概要

• 論文の詳細を見る
• Springer-Verlag Tokyoの論文
• 2003-09-01

著者

• Materna Verena

  Institute Of Pathology Charite Campus Mitte Humboldt University Berlin

• LAGE Hermann

  Institute of Pathology, Charite Campus Mitte Humboldt University Berlin

• Lage Hermann

  Institute Of Pathology Charite Campus Mitte Humboldt University Berlin

関連論文

• Homozygous mutation Arg_ Trp in the ABC-transporter encoding gene MRP2/cMOAT/ABCC2 causes Dubin-Johnson syndrome in a Caucasian patient

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