P042 Severe hyperbilirubinemia in a Caucasian child with UGT1A1 211 G>A heterozygous mutation. Issue 4 (6th October 2018)

Record Type:: Journal Article
Title:: P042 Severe hyperbilirubinemia in a Caucasian child with UGT1A1 211 G>A heterozygous mutation. Issue 4 (6th October 2018)
Main Title:: P042 Severe hyperbilirubinemia in a Caucasian child with UGT1A1 211 G>A heterozygous mutation
Authors:: Mastrangelo, G.
Trapani, S.
Serranti, D.
Indolfi, G.
Abstract:
Is Part Of:: Digestive and liver disease. Volume 50:Issue 4(2018)Supplement
Journal:: Digestive and liver disease
Issue:: Volume 50:Issue 4(2018)Supplement
Issue Display:: Volume 50, Issue 4 (2018)
Year:: 2018
Volume:: 50
Issue:: 4
Issue Sort Value:: 2018-0050-0004-0000
Page Start:: e373
Page End:: e374
Publication Date:: 2018-10-06
Subjects:: Digestive organs -- Diseases -- Periodicals
Liver -- Diseases -- Periodicals
616.33005
Journal URLs:: http://www.sciencedirect.com/science/journal/15908658 ↗
http://www.elsevier.com/journals ↗
DOI:: 10.1016/S1590-8658(18)31041-7 ↗
Languages:: English
ISSNs:: 1590-8658
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3588.345600
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 7767.xml