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. [electronic resource]
Producer: 20140408Description: 3391-7 p. digitalISSN:- 1676-5680
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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