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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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| Publicado no: | J Clin Res Pediatr Endocrinol |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Galenos Publishing
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6083467/ https://ncbi.nlm.nih.gov/pubmed/29537379 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4274/jcrpe.5506 |
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