共 6 条
[1]
Genotype of UGT1A1 and phenotype correlation between Crigler–Najjar syndrome type II and Gilbert syndrome.[J].Yoshihiro Maruo;Sayuri Nakahara;Takahide Yanagi;Akitaka Nomura;Yu Mimura;Katsuyuki Matsui;Hiroshi Sato;Yoshihiro Takeuchi.Journal of Gastroenterology and Hepatology.2016, 2
[3]
Role of a homozygous A(TA)₇TAA promoter polymorphism and an exon 1 heterozygous frameshift mutation UGT1A1 in Crigler-Najjar syndrome type II in a Thai neonate..[J].Nilyanimit P;Krasaelap A;Foonoi M;Chongsrisawat V;Poovorawan Y.Genetics and molecular research : GMR.2013, 3
[6]

