Associated Papers
Familial male-limited precocious puberty due to an activating mutation of the LHCGR: a case report and literature review.
Ha J et al.
Annals of Pediatric Endocrinology & Metabolism, 2024
A Case of Familial Male-limited Precocious Puberty with a Novel Mutation
Gurnurkar S et al.
Journal of Clinical Research in Pediatric Endocrinology, 2021
Novel C617Y mutation in the 7th transmembrane segment of luteinizing hormone/choriogonadotropin receptor in a Japanese boy with peripheral precocious puberty.
Nagasaki K et al.
Endocrine Journal, 2010
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