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Identification of a novel deletion in UDP-glucuronosyltransferase gene in a patient with Crigler-Najjar syndrome type I.
- Source :
-
Blood cells, molecules & diseases [Blood Cells Mol Dis] 2009 May-Jun; Vol. 42 (3), pp. 265-6. Date of Electronic Publication: 2009 Feb 13. - Publication Year :
- 2009
- Subjects :
- Adult
Amino Acid Sequence
Base Sequence
Exons genetics
Female
Genotype
Glucuronosyltransferase deficiency
Humans
Hyperbilirubinemia, Neonatal etiology
Hyperbilirubinemia, Neonatal genetics
Infant, Newborn
Male
Molecular Sequence Data
Pedigree
Crigler-Najjar Syndrome genetics
Glucuronosyltransferase genetics
Sequence Deletion
Subjects
Details
- Language :
- English
- ISSN :
- 1096-0961
- Volume :
- 42
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Blood cells, molecules & diseases
- Publication Type :
- Report
- Accession number :
- 19217809
- Full Text :
- https://doi.org/10.1016/j.bcmd.2008.12.004