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
Phenotypic Variability of Males with Loss-of-Function Mutations of <italic>MKRN3</italic>: A Case Report and Literature Review.
Yamanaka MYM et al.
Hormone Research in Paediatrics, 2025
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
A novel heterozygous MKRN3 nonsense mutation in a Chinese girl with idiopathic central precocious puberty: A case report.
Liu M et al.
Medicine, 2020
(Epi)genetic defects of MKRN3 are rare in Asian patients with central precocious puberty.
Suzuki E et al.
Human Genome Variation, 2019
Underdiagnosis of central precocious puberty in boys with loss-of-function mutations of MKRN3.
Brito VN et al.
The Journal of Pediatrics, 2017
Males with Paternally Inherited MKRN3 Mutations May Be Asymptomatic.
Dimitrova-Mladenova MS et al.
The Journal of Pediatrics, 2016
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