TY  - GEN
AU  - Kadakol,A
AU  - Sappal,B S
AU  - Ghosh,S S
AU  - Lowenheim,M
AU  - Chowdhury,A
AU  - Chowdhury,S
AU  - Santra,A
AU  - Arias,I M
AU  - Chowdhury,J R
AU  - Chowdhury,N R
TI  - Interaction of coding region mutations and the Gilbert-type promoter abnormality of the       UGT1A1 gene causes moderate degrees of unconjugated  hyperbilirubinaemia and may lead to       neonatal kernicterus
SN  - 1468-6244
PY  - 2001///1025
KW  - Adult
KW  - Animals
KW  - Base Sequence
KW  - Blotting, Western
KW  - COS Cells
KW  - Codon
KW  - genetics
KW  - Crigler-Najjar Syndrome
KW  - DNA
KW  - chemistry
KW  - DNA Mutational Analysis
KW  - Female
KW  - Gilbert Disease
KW  - Glucuronosyltransferase
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Jaundice, Neonatal
KW  - Kernicterus
KW  - Male
KW  - Mutation
KW  - Mutation, Missense
KW  - Plasmids
KW  - Promoter Regions, Genetic
N1  - Publication Type: Letter; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1136/jmg.38.4.244
ER  -