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Novel Melanocortin 2 Receptor Variant in a Chinese Infant With Familial Glucocorticoid Deficiency Type 1, Case Report and Review of Literature
Abuduxikuer, Kuerbanjiang; Li, Zhong-Die; Xie, Xin-Bao; Li, Yu-Chuan; Zhao, Jing; Wang, Jian-She
刊名FRONTIERS IN ENDOCRINOLOGY
2019
卷号10
关键词melanocortin 2 receptor (MC2R) familial glucocorticoid deficiency (FGD) type 1 cholestasis skin hyperpigmentation hypoglycemia cortisol adrenocorticotropic hormone (ACTH) linear overgrowth
ISSN号1664-2392
URL标识查看原文
语种英语
内容类型期刊论文
URI标识http://www.corc.org.cn/handle/1471x/3598991
专题复旦大学上海医学院
推荐引用方式
GB/T 7714
Abuduxikuer, Kuerbanjiang,Li, Zhong-Die,Xie, Xin-Bao,et al. Novel Melanocortin 2 Receptor Variant in a Chinese Infant With Familial Glucocorticoid Deficiency Type 1, Case Report and Review of Literature[J]. FRONTIERS IN ENDOCRINOLOGY,2019,10.
APA Abuduxikuer, Kuerbanjiang,Li, Zhong-Die,Xie, Xin-Bao,Li, Yu-Chuan,Zhao, Jing,&Wang, Jian-She.(2019).Novel Melanocortin 2 Receptor Variant in a Chinese Infant With Familial Glucocorticoid Deficiency Type 1, Case Report and Review of Literature.FRONTIERS IN ENDOCRINOLOGY,10.
MLA Abuduxikuer, Kuerbanjiang,et al."Novel Melanocortin 2 Receptor Variant in a Chinese Infant With Familial Glucocorticoid Deficiency Type 1, Case Report and Review of Literature".FRONTIERS IN ENDOCRINOLOGY 10(2019).
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