Associated Papers
Makorin RING finger protein 3 and central precocious puberty.
Maione L et al.
Current Opinion in Endocrine and Metabolic Research, 2020
(Epi)genetic defects of MKRN3 are rare in Asian patients with central precocious puberty.
Suzuki E et al.
Human Genome Variation, 2019
Investigation of MKRN3 Mutation in Patients with Familial Central Precocious Puberty
Aycan Z et al.
Journal of Clinical Research in Pediatric Endocrinology, 2018
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