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A homozygous mutation in the insulin gene (INS) causing autosomal recessive neonatal diabetes in Saudi families
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 insulin biosynthesis through distinct mechanisms. In this study, we report a homozygous mutat...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Korean Society of Pediatric Endocrinology
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7136508/ https://www.ncbi.nlm.nih.gov/pubmed/32252216 http://dx.doi.org/10.6065/apem.2020.25.1.42 |