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Cited by in CrossRef
For: Jiang LQ, Zhou YQ, Yuan K, Zhu JF, Fang YL, Wang CL. Rare mutation in MKRN3 in two twin sisters with central precocious puberty: Two case reports. World J Clin Cases 2021; 9(32): 10018-10023 [PMID: 34877345 DOI: 10.12998/wjcc.v9.i32.10018]
URL: https://www.wjgnet.com/2307-8960/full/v9/i32/10018.htm
Number Citing Articles
1
Ziwei Chen, Wenying Li, Junqi Wang, Zhiya Dong, Chuanyin Li, Wei Wang, Ronggui Hu, Xiaoyu Ma, Yuan Xiao, Wenli Lu, Suraiya Saleem. Outcomes of Patients With Familial Central Precocious Puberty due to Mutations of MKRN3 Gene After Treatment With Gonadotropin‐Releasing Hormone AgonistInternational Journal of Endocrinology 2025; 2025(1) doi: 10.1155/ije/5609749