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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
Author(s) -
Labrune Philippe,
Myara Anne,
Chalas Jacqueline,
Le Bihan Béatrice,
Capel Liliane,
Francoual Jeanne
Publication year - 2002
Publication title -
human mutation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 162
eISSN - 1098-1004
pISSN - 1059-7794
DOI - 10.1002/humu.10122
Subject(s) - microbiology and biotechnology , stereochemistry , genetics , chemistry , biology