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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