MKRN3 circulating levels in girls with central precocious puberty caused by MKRN3 gene mutations
Author:
Funder
Università degli Studi della Campania Luigi Vanvitelli
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
https://link.springer.com/content/pdf/10.1007/s40618-023-02255-5.pdf
Reference36 articles.
1. Avendaño MS, Vazquez MJ, Tena-Sempere M (2017) Disentangling puberty: novel neuroendocrine pathways and mechanisms for the control of mammalian puberty. Hum Reprod Update. https://doi.org/10.1093/humupd/dmx025. (PMID: 28961976)
2. Brito VN, Canton APM, Seraphim CE, Abreu AP, Macedo DB, Mendonca BB, Kaiser UB, Argente J, Latronico AC (2022) The congenital and acquired mechanisms implicated in the etiology of central precocious puberty. Endocr Rev. https://doi.org/10.1210/endrev/bnac020. (Epub ahead of print. PMID: 35930274)
3. Tinano FR, Canton APM, Montenegro LR, de Castro LA, Faria AG, Seraphim CE, Brauner R, Jorge AA, Mendonca BB, Argente J, Brito VN, Latronico AC (2023) Clinical and genetic characterization of familial central precocious puberty. J Clin Endocrinol Metab. https://doi.org/10.1210/clinem/dgac763
4. Valadares LP, Meireles CG, De Toledo IP et al (2019) MKRN3 Mutations in central precocious puberty: a systematic review and meta-analysis. J Endocr Soc. https://doi.org/10.1210/js.2019-00041
5. Tinano FR, Canton APM, Montenegro LR et al (2023) Clinical and genetic characterization of familial central precocious puberty. J Clin Endocrinol Metab. https://doi.org/10.1210/clinem/dgac763
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