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...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Pubblicato in:J Clin Endocrinol Metab
Autori principali: 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
Natura: Artigo
Lingua:Inglês
Pubblicazione: Endocrine Society 2017
Soggetti:
Clinical Research Articles
Accesso online: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
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !

Documenti analoghi