Congenital Hyperinsulinism Caused by Novel Homozygous KATP Channel Gene Variants May Be Linked to Unexplained Neonatal Deaths among Kurdish Consanguineous Families

标题
Congenital Hyperinsulinism Caused by Novel Homozygous KATP Channel Gene Variants May Be Linked to Unexplained Neonatal Deaths among Kurdish Consanguineous Families
作者
关键词
-
出版物
Hormone Research in Paediatrics
Volume -, Issue -, Pages 1-8
出版商
S. Karger AG
发表日期
2020-03-24
DOI
10.1159/000506476

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