Abstract |
|
Authors | Aria Setoodeh, Ali Rabbani |
Journal | Acta medica Iranica
(Acta Med Iran)
Vol. 50
Issue 12
Pg. 836-8
( 2012)
ISSN: 1735-9694 [Electronic] Iran |
PMID | 23456528
(Publication Type: Case Reports, Journal Article)
|
Copyright | © 2012 Tehran University of Medical Sciences. All rights reserved. |
Chemical References |
- Glucose Transporter Type 2
- Hypoglycemic Agents
- Insulin
- SLC2A2 protein, human
|
Topics |
- Child
- Consanguinity
- DNA Mutational Analysis
- Diabetes Mellitus
(diagnosis, drug therapy, etiology)
- Diabetic Ketoacidosis
(drug therapy, etiology)
- Fanconi Syndrome
(complications, diagnosis, genetics, therapy)
- Female
- Genetic Predisposition to Disease
- Glucose Transporter Type 2
(genetics)
- Humans
- Hypoglycemic Agents
(therapeutic use)
- Infant, Newborn
- Insulin
(therapeutic use)
- Mutation
- Phenotype
|