Associated Papers
MKRN3 and KISS1R mutations in precocious and early puberty.
Pagani S et al.
Italian Journal of Pediatrics, 2020
Clinical Exome Sequencing Reveals MKRN3 Pathogenic Variants in Familial and Nonfamilial Idiopathic Central Precocious Puberty.
Ortiz-Cabrera NV et al.
Hormone Research in Paediatrics, 2017
MKRN3 mutations in familial central precocious puberty.
Schreiner F et al.
Hormone Research in Paediatrics, 2014
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