Absence of Functional LIN28B Mutations in a Large Cohort of Patients with Idiopathic Central Precocious Puberty

AIM: To investigate LIN28B gene variants in children with idiopathic central precocious puberty (CPP). PATIENTS AND METHODS: We studied 178 Brazilian children with CPP (171 girls,16.8% familial cases). A large multiethnic group (1599 subjects; MEC cohort) was used as control. DNA analysis and bioche...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Silveira-Neto, Acácio P., Leal, Leticia Ferro, Emerman, Amy B., Henderson, Katherine D., Piskounova, Elena, Henderson, Brian E., Gregory, Richard I., Gontijo Silveira, Letícia F., Hirschhorn, Joel N., Nguyen, Thutrang T., Beneduzzi, Daiane, Tusset, Cintia, Reis, Ana Claudia S., Brito, Vinicius N., Mendonça, Berenice B., Palmert, Mark R, Antonini, Sonir R, Latronico, Ana Claudia
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2012
Pynciau:
Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC3526815/
https://ncbi.nlm.nih.gov/pubmed/22964795
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000342212
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