- A homozygous mutation in the insulin gene (INS) causing autosomal recessive neonatal diabetes in Saudi families
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Shaikh AA, Shirah B, Alzelaye S
- KMID: 2501036
- Ann Pediatr Endocrinol Metab.
- 2020 Mar;25(1):42-45.
- doi: 10.6065/apem.2020.25.1.42
Purpose: Insulin gene (INS) mutations are a rare cause of permanent neonatal diabetes and mature-onset diabetes of the young (MODY10). Homozygous mutations have been reported to cause diabetes by decreasing... -
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