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Crigler–Najjar type II syndrome may result from several types and combinations of mutations in the UGT1A1 gene
Author(s) -
Petit F,
Gajdos V,
Capel L,
Parisot F,
Myara A,
Francoual J,
Labrune P
Publication year - 2006
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.2006.00616.x
Subject(s) - medicine , chemistry
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