Načítá se...

AB077. Clinical symptoms, molecular genetics, genotype and phenotype correlations of children with congenital hyperinsulinism

BACKGROUND AND OBJECTIVE: Congenital hyperinsulinism (HI) causes severe hypoglycemia in neonates and infants. Molecular genetic results is very important which help clinicians will have suitable treatment. The study aims to describe clinical symptoms, signs of HI patients and to identify mutations i...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:Ann Transl Med
Hlavní autoři: Duong, Dang Anh, Dung, Vu Chi, Dat, Nguyen Phu, Ngoc, Can Thi Bich, Thao, Bui Phuong, Khanh, Nguyen Ngoc, Dien, Tran Minh
Médium: Artigo
Jazyk:Inglês
Vydáno: AME Publishing Company 2015
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4563418/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3978/j.issn.2305-5839.2015.AB077
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!