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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| Main Authors: | , , |
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| Format: | Book |
| Published: |
Korean Society of Pediatric Endocrinology,
2020-03-01T00:00:00Z.
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| Subjects: | |
| Online Access: | Connect to this object online. |
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |