The type 2 diabetes presumed causal variant within TCF7L2 resides in an element that controls the ex...
The type 2 diabetes presumed causal variant within TCF7L2 resides in an element that controls the expression of ACSL5
About this item
Full title
Author / Creator
Publisher
Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title
Language
English
Formats
Publication information
Publisher
Berlin/Heidelberg: Springer Berlin Heidelberg
Subjects
More information
Scope and Contents
Contents
Aims/hypothesis
One of the most strongly associated type 2 diabetes loci reported to date resides within the
TCF7L2
gene. Previous studies point to the T allele of rs7903146 in intron 3 as the causal variant at this locus. We aimed to identify the actual gene(s) under the influence of this variant.
Methods
Using clustered regularly i...
Alternative Titles
Full title
The type 2 diabetes presumed causal variant within TCF7L2 resides in an element that controls the expression of ACSL5
Authors, Artists and Contributors
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_proquest_miscellaneous_1827932044
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1827932044
Other Identifiers
ISSN
0012-186X
E-ISSN
1432-0428
DOI
10.1007/s00125-016-4077-2
