Allelic heterogeneity of Crigler-Najjar type I syndrome: a study of 24 cases
Clin Genet
.
2004 Dec;66(6):571-2.
doi: 10.1111/j.1399-0004.2004.00371.x.
Authors
F M Petit
,
V Gajdos
,
J Francoual
,
L Capel
,
F Parisot
,
C Poüs
,
P Labrune
PMID:
15521991
DOI:
10.1111/j.1399-0004.2004.00371.x
No abstract available
Publication types
Letter
MeSH terms
Crigler-Najjar Syndrome / genetics*
Glucuronosyltransferase / genetics
Humans
Hyperbilirubinemia, Hereditary / genetics*
Infant, Newborn
Mutation
Substances
UGT1A1 enzyme
Glucuronosyltransferase