A case of familial central precocious puberty caused by a novel mutation in the makorin RING finger protein 3 gene

BACKGROUND: Central precocious puberty (CPP) is often familial but its genetic cause is largely unknown. Very recently, the makorin RING finger protein 3 (MKRN3) gene, located on chromosome 15 in the Prader-Willi syndrome (PWS)-associated region (15q11-q13), has been found mutated in 5 families with...

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Detalles Bibliográficos
Autores principales: Grandone, Anna, Cantelmi, Grazia, Cirillo, Grazia, Marzuillo, Pierluigi, Luongo, Caterina, Miraglia del Giudice, Emanuele, Perrone, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4619005/
https://www.ncbi.nlm.nih.gov/pubmed/26499472
http://dx.doi.org/10.1186/s12902-015-0056-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4619005/
https://www.ncbi.nlm.nih.gov/pubmed/26499472
http://dx.doi.org/10.1186/s12902-015-0056-8

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