Congenital hyperinsulinemia and diabetes caused by ABCC8 variant in a family: a case report

Ping Yang; Sihan Wang; Hongmin Xi; Xiangyun Yin; Lili Ma; Liangliang Li; Mengya Sun; Hong Jiang; Xianghong Li

doi:10.1093/qjmed/hcae217

Congenital hyperinsulinemia and diabetes caused by ABCC8 variant in a family: a case report

Ping Yang
, Sihan Wang
, Hongmin Xi
, Xiangyun Yin
, Lili Ma
, Liangliang Li
, Mengya Sun
, Hong Jiang
, Xianghong Li

Qingdao University

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	123-125
Number of pages	3
Journal	QJM: An International Journal of Medicine
Volume	118
Issue number	2
DOIs	https://doi.org/10.1093/qjmed/hcae217
State	Published - 1 Feb 2025
Externally published	Yes

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10.1093/qjmed/hcae217

Cite this

@article{9fee263038864ae589c6ea41bb2bd8ba,

title = "Congenital hyperinsulinemia and diabetes caused by ABCC8 variant in a family: a case report",

author = "Ping Yang and Sihan Wang and Hongmin Xi and Xiangyun Yin and Lili Ma and Liangliang Li and Mengya Sun and Hong Jiang and Xianghong Li",

year = "2025",

month = feb,

day = "1",

doi = "10.1093/qjmed/hcae217",

language = "英语",

volume = "118",

pages = "123--125",

journal = "QJM: An International Journal of Medicine",

issn = "1460-2725",

publisher = "Oxford University Press",

number = "2",

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TY - JOUR

T1 - Congenital hyperinsulinemia and diabetes caused by ABCC8 variant in a family

T2 - a case report

AU - Yang, Ping

AU - Wang, Sihan

AU - Xi, Hongmin

AU - Yin, Xiangyun

AU - Ma, Lili

AU - Li, Liangliang

AU - Sun, Mengya

AU - Jiang, Hong

AU - Li, Xianghong

PY - 2025/2/1

Y1 - 2025/2/1

UR - https://www.scopus.com/pages/publications/105001189254

U2 - 10.1093/qjmed/hcae217

DO - 10.1093/qjmed/hcae217

M3 - 文章

C2 - 39514111

AN - SCOPUS:105001189254

SN - 1460-2725

VL - 118

SP - 123

EP - 125

JO - QJM: An International Journal of Medicine

JF - QJM: An International Journal of Medicine

IS - 2

ER -

Congenital hyperinsulinemia and diabetes caused by ABCC8 variant in a family: a case report

UN SDGs

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