Novel deletion mutation in the glucokinase gene from a Korean man with GCK-MODY phenotype and situs inversus. (September 2018)
- Record Type:
- Journal Article
- Title:
- Novel deletion mutation in the glucokinase gene from a Korean man with GCK-MODY phenotype and situs inversus. (September 2018)
- Main Title:
- Novel deletion mutation in the glucokinase gene from a Korean man with GCK-MODY phenotype and situs inversus
- Authors:
- Cho, Yun Kyung
Cho, Eun-Hee
Choi, Hoon Sung
Kim, Sang-Wook - Abstract:
- Abstract: A novel mutation in intron 9–exon 10 boundary of the GCK gene was detected in a male patient with clinical features of GCK-MODY and situs inversus. This case highlights the value of sequencing the GCK gene in individuals with GCK-MODY phenotype and no family history of monogenic diabetes.
- Is Part Of:
- Diabetes research and clinical practice. Volume 143(2018)
- Journal:
- Diabetes research and clinical practice
- Issue:
- Volume 143(2018)
- Issue Display:
- Volume 143, Issue 2018 (2018)
- Year:
- 2018
- Volume:
- 143
- Issue:
- 2018
- Issue Sort Value:
- 2018-0143-2018-0000
- Page Start:
- 263
- Page End:
- 266
- Publication Date:
- 2018-09
- Subjects:
- Glucokinase -- Maturity-onset diabetes of the young -- Situs inversus
Diabetes -- Periodicals
Diabetes Mellitus -- Periodicals
616.462 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01688227 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/01688227 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/01688227 ↗
http://www.sciencedirect.com/science/journal/01688227 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.diabres.2018.07.036 ↗
- Languages:
- English
- ISSNs:
- 0168-8227
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3579.603700
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 11588.xml