Associated Papers
Divergent epigenetic profile underlie pubertal disorders in MKRN3-associated central precocious puberty and Prader-Willi syndrome: insights from a frameshift variant.
Jin YY et al.
World Journal of Pediatrics : Wjp, 2026
Novel MKRN3 gene mutation associated with central precocious puberty in a Chinese child: a case report.
Wang J et al.
Frontiers in Endocrinology, 2024
Genetic causes of central precocious puberty.
Tajima T
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology, 2022
Familial central precocious puberty: two novel MKRN3 mutations.
Varimo T et al.
Pediatric Research, 2021
Makorin RING finger protein 3 and central precocious puberty.
Maione L et al.
Current Opinion in Endocrine and Metabolic Research, 2020
MKRN3 Mutations in Central Precocious Puberty: A Systematic Review and Meta-Analysis.
Valadares LP et al.
Journal of the Endocrine Society, 2019
High Frequency of MKRN3 Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic.
Bessa DS et al.
Neuroendocrinology, 2017
Low Frequency of MKRN3 Mutations in Central Precocious Puberty Among Korean Girls.
Lee HS et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme, 2016
Select a paper to view details