- Abstract:
-
There are well-documented examples in the literature of where determining the genetic aetiology of a disorder has provided insights into important regulatory pathways and protein interactions, and, more recently, has led to improved treatment options for patients. The studies of monogenic forms of beta-cell dysfunction are no exception. Naturally occurring mutations in the gene for the beta-cell enzyme glucokinase (GCK) result in both hyper- and hypo-glycaemia. Over 200 mutations have been de...
Expand abstract - Publication status:
- Published
- Publisher copy:
- 10.1042/bst0360306
-
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- Journal:
- Biochemical Society transactions
- Volume:
- 36
- Issue:
- Pt 3
- Pages:
- 306-311
- Publication date:
- 2008-06-05
- DOI:
- EISSN:
-
1470-8752
- ISSN:
-
0300-5127
- URN:
-
uuid:e1778676-8b8c-4c8c-859f-38d30c09471b
- Source identifiers:
-
9453
- Local pid:
- pubs:9453
- Language:
- English
- Keywords:
- Copyright date:
- 2008
Journal article
Glucokinase (GCK) and other susceptibility genes for beta-cell dysfunction: the candidate approach.
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