Associated Papers
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
Six Novel Variants in the MKRN3 Gene Causing Central Precocious Puberty.
Gernay C et al.
Journal of the Endocrine Society, 2022
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