Analysis of large‐scale sequencing cohorts does not support the role of variants in UCP2 as a cause of hyperinsulinaemic hypoglycaemia. Issue 10 (1st August 2017)

Record Type:: Journal Article
Title:: Analysis of large‐scale sequencing cohorts does not support the role of variants in UCP2 as a cause of hyperinsulinaemic hypoglycaemia. Issue 10 (1st August 2017)
Main Title:: Analysis of large‐scale sequencing cohorts does not support the role of variants in UCP2 as a cause of hyperinsulinaemic hypoglycaemia
Authors:: Laver, Thomas W
Weedon, Michael N
Caswell, Richard
Hussain, Khalid
Ellard, Sian
Flanagan, Sarah E
Abstract:
Is Part Of:: Human mutation. Volume 38:Issue 10(2017)
Journal:: Human mutation
Issue:: Volume 38:Issue 10(2017)
Issue Display:: Volume 38, Issue 10 (2017)
Year:: 2017
Volume:: 38
Issue:: 10
Issue Sort Value:: 2017-0038-0010-0000
Page Start:: 1442
Page End:: 1444
Publication Date:: 2017-08-01
Subjects:: congenital hyperinsulinism -- genetics -- hypoglycaemia -- UCP2
Human chromosome abnormalities -- Periodicals
Mutation (Biology) -- Periodicals
616.04205
Journal URLs:: http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1098-1004 ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1002/humu.23289 ↗
Languages:: English
ISSNs:: 1059-7794
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 4336.217000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 4684.xml