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Crigler-najjar Syndrome Type Ii Caused by a Homozygous Triple Mutation [t-3279g, A(ta)7taa, and H39d] of ugt1a1
Crigler-najjar Syndrome Type Ii Caused by a Homozygous Triple Mutation [t-3279g, A(ta)7taa, and H39d] of ugt1a1
2006
Yoshihiro Maruo
Ali Kemal Topaloglu
Hiroko Takahashi
Asami Mori
Masaru Iwai
Oznur Duzovali
Kazuo Yamamoto
Katsuyuki Matui
Hiroshi Sato
Yoshihiro Takeuchi
Keywords:
Crigler-najjar disease
Gastroenterology
Diabetes mellitus
Endocrinology
Mutation
Crigler-Najjar syndrome type II
Medicine
Internal medicine
biliary tract disease
Correction
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