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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Xehetasun bibliografikoak
Argitaratua izan da:Ann Transl Med
Egile Nagusiak: Duong, Dang Anh, Dung, Vu Chi, Dat, Nguyen Phu, Ngoc, Can Thi Bich, Thao, Bui Phuong, Khanh, Nguyen Ngoc, Dien, Tran Minh
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: AME Publishing Company 2015
Gaiak:
Part 4: Oral/poster
Sarrera elektronikoa: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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