Congenital Hyperinsulinism Due to Compound Heterozygous Mutation in ABCC8 and KCNJ11 GENES: 20 Years Experience of A National Referral Centre

被引：0
|
作者：
Walton-Betancourth, Sandra [1 ]
Shah, Pratik [1 ,2 ]
Flanagan, Sarah [3 ]
Ellard, Sian [3 ]
Guemes, Maria [1 ,2 ]
Gilbert, Clare [1 ]
Silvera, Shavel [1 ]
Hussain, Khalid [1 ,2 ]
机构：
[1] Great Ormond St Hosp Sick Children, London Ctr Paediat Endocrinol, London, England
[2] UCL, Inst Child Hlth, Dev Endocrinol Res Grp, Genet & Genom Med, London, England
[3] Univ Exeter, Inst Biomed & Clin Sci, Sch Med, Exeter, Devon, England
来源：
HORMONE RESEARCH IN PAEDIATRICS | 2016年 / 86卷
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
P1-P560
引用
收藏
页码：348 / 348
页数：1
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