[1]于之瑶 李静.合并线粒体基因突变及中枢神经系统损害的2型糖尿病 1例家系报告及文献复习[J].国际内分泌代谢杂志,2020,40(04):279-283.[doi:10.3760/cma.j.issn.1673-4157.2020.04.015]
 Yu Zhiyao,Li Jing.A family of type 2 diabetes mellitus with mitochondrial gene mutation and impairment of nervous system: a case report and literatures review[J].International Journal of Endocrinology and Metabolism,2020,40(04):279-283.[doi:10.3760/cma.j.issn.1673-4157.2020.04.015]
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合并线粒体基因突变及中枢神经系统损害的2型糖尿病 1例家系报告及文献复习
分享到:

《国际内分泌代谢杂志》[ISSN:1673-4157/CN:12-1383/R]

卷:
40
期数:
2020年04期
页码:
279-283
栏目:
病例报告
出版日期:
2020-07-20

文章信息/Info

Title:
A family of type 2 diabetes mellitus with mitochondrial gene mutation and impairment of nervous system: a case report and literatures review
作者:
于之瑶 李静
中国医科大学附属第一医院内分泌科 110001
Author(s):
Yu Zhiyao Li Jing
Department of Endocrinology, The First Hospital of China Medical University, Shenyang 110001, China
DOI:
10.3760/cma.j.issn.1673-4157.2020.04.015

参考文献/References:

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[11] Liou CW,Lin TK,Huei WH,et al. A common mitochondrial DNA variant and increased body mass index as associated factors for development of type 2 diabetes:additive effects of genetic and environmental factors[J].J Clin Endocrinol Metab,2007,92(1):235-239.DOI:10.1210/jc.2006-0653.
[12] Ye Z,Gillson C,Sims M,et al. The association of the mitochondrial DNA OriB variant(16184-16193 polycytosine tract)with type 2 diabetes in Europid populations[J].Diabetologia,2013,56(9):1907-1913.DOI:10.1007/s00125-013-2945-6.
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备注/Memo

备注/Memo:
通信作者:李静,Email:lijingendocrine@126.com
基金项目:国家重点研发计划(2017YFC0907403); 国家自然科学基金(81771741); 辽宁省教育厅第四批辽宁特聘教授人才项目(辽教发2014-187号)
Corresponding author:Li Jing, Email:lijingendocrine@126.com
Corresponding author:Li Jing, Email:lijingendocrine@126.com
Fund program:The National Key Research and Development Program of China(2017YFC0907403); National Natural Science Foundation of China(81771741); Distinguished Professor at Educational Department of Liaoning Province([2014]187)
更新日期/Last Update: 2020-07-20