Novel Mutation in Wolcott–Rallison Syndrome with Variable Expression in Two Omani Siblings
Wolcott-Rallison syndrome (WRS) is an autosomal recessive disease, characterized by neonatal or early-onset non-autoimmune insulin-dependent diabetes. WRS, although rare, is recognized to be the most frequent cause of neonatal-onset diabetes. The majority of reported patients are from consanguineous...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Oman Medical Specialty Board
2015-03-01
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| Series: | Oman Medical Journal |
| Subjects: | |
| Online Access: | http://www.omjournal.org/fultext_PDF.aspx?DetailsID=634&type=fultext |