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
Familial central precocious puberty: two novel MKRN3 mutations.
Varimo T et al.
Pediatric Research, 2021
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