APA

Nakagawa T., Mure T., Yusoff S., Ono E., Kusuma Harahap I. S., Morikawa S., Morioka I., Takeshima Y., Nishio H. & Matsuo M. (20120404). A homozygous mutation in UGT1A1 exon 5 may be responsible for persistent hyperbilirubinemia in a Japanese girl with Gilbert's syndrome. : The Kobe journal of medical sciences.

Chicago

Nakagawa Taku, Mure Takeo, Yusoff Surini, Ono Eiichi, Kusuma Harahap Indra Sari, Morikawa Satoru, Morioka Ichiro, Takeshima Yasuhiro, Nishio Hisahide and Matsuo Masafumi. 20120404. A homozygous mutation in UGT1A1 exon 5 may be responsible for persistent hyperbilirubinemia in a Japanese girl with Gilbert's syndrome. : The Kobe journal of medical sciences.

Harvard

Nakagawa T., Mure T., Yusoff S., Ono E., Kusuma Harahap I. S., Morikawa S., Morioka I., Takeshima Y., Nishio H. and Matsuo M. (20120404). A homozygous mutation in UGT1A1 exon 5 may be responsible for persistent hyperbilirubinemia in a Japanese girl with Gilbert's syndrome. : The Kobe journal of medical sciences.

MLA

Nakagawa Taku, Mure Takeo, Yusoff Surini, Ono Eiichi, Kusuma Harahap Indra Sari, Morikawa Satoru, Morioka Ichiro, Takeshima Yasuhiro, Nishio Hisahide and Matsuo Masafumi. A homozygous mutation in UGT1A1 exon 5 may be responsible for persistent hyperbilirubinemia in a Japanese girl with Gilbert's syndrome. : The Kobe journal of medical sciences. 20120404.