The clinical and genetic characterisation of young-onset diabetes
<p>Maturity-onset diabetes of the young (MODY), due to hepatocyte nuclear factor 1 alpha mutations (HNF1A-MODY), is the most common form of monogenic diabetes presenting in young adults. An accurate genetic diagnosis of HNF1A-MODY has therapeutic implications for the patients and their family...
Príomhchruthaitheoir: | Mughal, S |
---|---|
Rannpháirtithe: | Owen, K |
Formáid: | Tráchtas |
Teanga: | English |
Foilsithe / Cruthaithe: |
2014
|
Ábhair: |
Míreanna comhchosúla
Míreanna comhchosúla
-
The role of genetic variation in glucokinase and glucokinase regulatory protein in diabetes and related traits
de réir: Beer, N, et al.
Foilsithe / Cruthaithe: (2011) -
Mechanisms of Type 2 diabetes susceptibility
de réir: Travers, M, et al.
Foilsithe / Cruthaithe: (2013) -
The role of glucose-6-phosphatase catalytic domain in glucose homeostasis
de réir: Ng, NHJ
Foilsithe / Cruthaithe: (2016) -
The role of the G-protein subunit, G-alpha-11, and the adaptor protein 2 sigma subunit, ap2-sigma-2, in the regulation of calcium homeostasis
de réir: Howles, S
Foilsithe / Cruthaithe: (2015) -
Gene modifiers and novel therapies for multiple endocrine neoplasia type 1
de réir: Javid, M
Foilsithe / Cruthaithe: (2012)