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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...

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Detalles Bibliográficos
Autores principales:	Shaikh, Adnan Al, Shirah, Bader, Alzelaye, Somaya
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Korean Society of Pediatric Endocrinology 2020
Materias:	Original Article
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

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