AB078. Novel mutation of ABCC8 and KCNJ11 of children with congenital hyperinsulinism

BACKGROUND AND OBJECTIVE: Congenital hyperinsulinism (HI) causes severe hypoglycemia in neonates and infants. To date, more than 350 mutations have been reported in HI patients. However, the genetic screening has failed to define the genetic basis of disease in more than 18% of the cases, demonstrat...

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Bibliografske podrobnosti
izdano v:Ann Transl Med
Main Authors: Duong, Dang Anh, Dung, Vu Chi, Dat, Nguyen Phu, Ngoc, Can Thi Bich, Thao, Bui Phuong, Khanh, Nguyen Ngoc, Dien, Tran Minh
Format: Artigo
Jezik:Inglês
Izdano: AME Publishing Company 2015
Teme:
Part 4: Oral/poster
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC4563494/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3978/j.issn.2305-5839.2015.AB078
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