Investigation of MKRN3 Mutation in Patients with Familial Central Precocious Puberty

OBJECTIVE: There have been recent advances in the understanding of the etiology of idiopathic central precocious puberty (iCPP) including new genetic associations. The aim of this clinical study was to determine the frequency of MKRN3 mutation in cases of familial iCPP. METHODS: Potential sequence v...

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Detalles Bibliográficos
Autores principales: Aycan, Zehra, Savaş-Erdeve, Şenay, Çetinkaya, Semra, Kurnaz, Erdal, Keskin, Melikşah, Muratoğlu Şahin, Nursel, Bayramoğlu, Elvan, Ceylaner, Gülay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2018
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6083467/
https://www.ncbi.nlm.nih.gov/pubmed/29537379
http://dx.doi.org/10.4274/jcrpe.5506

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6083467/
https://www.ncbi.nlm.nih.gov/pubmed/29537379
http://dx.doi.org/10.4274/jcrpe.5506

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