Wolcott-Rallison syndrome due to the same mutation in EIF2AK3 (c.205G>T) in two unrelated families: A case report.

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作者： Ai,Huang ^[1] ; Haiyan,Wei ^[1]

作者单位： Department of Endocrinology, Children's Hospital Affiliated to Zhengzhou University, Henan Children's Hospital, Zhengzhou Children's Hospital, Zhengzhou, Henan 450018, P.R. China. ^[1]

关键词 Wolcott-Rallison syndrome eukaryotic translation initiation factor 2α kinase 3 liver failure neonatal diabetes mellitus

DOI 10.3892/etm.2019.7268

PMID 30906465

发布时间 2020-10-01

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Experimental and therapeutic medicine

2019年17卷4期

2765-2768页

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Wolcott-Rallison syndrome due to the same mutation in EIF2AK3 (c.205G>T) in two unrelated families: A case report.

Experimental and therapeutic medicine

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Experimental and therapeutic medicine

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Wolcott-Rallison syndrome due to the same mutation in EIF2AK3 (c.205G&gt;T) in two unrelated families: A case report.

Experimental and therapeutic medicine

相似文献

Experimental and therapeutic medicine

相关期刊

检索历史清除

Wolcott-Rallison syndrome due to the same mutation in EIF2AK3 (c.205G>T) in two unrelated families: A case report.