A homozygous mutation in the insulin gene () 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 mutati...
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| Автори: | , , |
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| Формат: | Книга |
| Опубліковано: |
Korean Society of Pediatric Endocrinology,
2020-03-01T00:00:00Z.
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| Онлайн доступ: | Connect to this object online. |
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Connect to this object online.3rd Floor Main Library
| Шифр: |
A1234.567 |
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| Примірник 1 | Доступно |