Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty

CONTEXT: Central precocious puberty (CPP) results from premature activation of the hypothalamic–pituitary–gonadal axis. Few genetic causes of CPP have been identified, with the most common being mutations in the paternally expressed imprinted gene MKRN3. OBJECTIVE: To identify the genetic etiology o...

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Detalhes bibliográficos
Publicado no:J Clin Endocrinol Metab
Main Authors: Dauber, Andrew, Cunha-Silva, Marina, Macedo, Delanie B., Brito, Vinicius N., Abreu, Ana Paula, Roberts, Stephanie A., Montenegro, Luciana R., Andrew, Melissa, Kirby, Andrew, Weirauch, Matthew T., Labilloy, Guillaume, Bessa, Danielle S., Carroll, Rona S., Jacobs, Dakota C., Chappell, Patrick E., Mendonca, Berenice B., Haig, David, Kaiser, Ursula B., Latronico, Ana Claudia
Formato: Artigo
Idioma:Inglês
Publicado em: Endocrine Society 2017
Assuntos:
Clinical Research Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5443333/
https://ncbi.nlm.nih.gov/pubmed/28324015
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2016-3677
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