| 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] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v9/i32/10018.htm |
| Number | Citing Articles |
| 1 |
Marcelo Yuji de Moura Yamanaka, Luciana R. Montenegro, Ana Pinheiro Machado Canton, Aline Almeida Bastos, Larissa Baracho Macena, Vinicius Nahime Brito, Ana Claudia Latronico. Phenotypic Variability of Males with Loss-of-Function Mutations of MKRN3: A Case Report and Literature Review. Hormone Research in Paediatrics 2025; : 1 doi: 10.1159/000549607
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| 2 |
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 Agonist. International Journal of Endocrinology 2025; 2025(1) doi: 10.1155/ije/5609749
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