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Central precocious puberty in a boy with pseudohypoparathyroidism type Ia due to a novel GNAS mutation

Detalles Bibliográficos
Autores principales:	Kagami, Ryosuke, Sato, Takeshi, Ishii, Tomohiro, Araki, Eriko, Yamashita, Yukio, Shibata, Hironori, Ishihara, Jun, Hasegawa, Tomonobu
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Japanese Society for Pediatric Endocrinology 2020
Materias:	Mutation-in-Brief
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160456/ https://www.ncbi.nlm.nih.gov/pubmed/32313379 http://dx.doi.org/10.1297/cpe.29.89

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