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Association of a homozygous (TA)8 promoter polymorphism and a N400D mutation of UGT1A1 in a child with Crigler-Najjar type II syndrome

✍ Scribed by Philippe Labrune; Anne Myara; Jacqueline Chalas; Béatrice Le Bihan; Liliane Capel; Jeanne Francoual


Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
132 KB
Volume
20
Category
Article
ISSN
1059-7794

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