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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Bibliografske podrobnosti
izdano v: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
Format: Artigo
Jezik:Inglês
Izdano: Endocrine Society 2017
Teme:
Clinical Research Articles
Online dostop: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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