Open AccessAbsence of Functional <b><i>LIN28B</i></b> Mutations in a Large Cohort of Patients with Idiopathic Central Precocious Puberty
Author(s) -
A. P. Silveira-Neto,
Letícia Ferro Leal,
Amy B. Emerman,
Katherine D. Henderson,
Elena Piskounova,
Brian E. Henderson,
Richard I. Gregory,
Letícia Ferreira Gontijo Silveira,
Joel N. Hirschhorn,
Thutrang Nguyen,
Daiane Beneduzzi,
Cíntia Tusset,
Ana Claudia S. Reis,
Vinícius Nahime Brito,
Berenice B. Mendonça,
Mark R. Palmert,
Sonir Roberto Rauber Antonini,
Ana Claudia Latrônico
Publication year - 2012
Publication title -
hormone research in paediatrics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.816
H-Index - 89
eISSN - 1663-2826
pISSN - 1663-2818
DOI - 10.1159/000342212
Subject(s) - cohort , biology , mutation , pathogenesis , microrna , genetics , medicine , single nucleotide polymorphism , endocrinology , gene , genotype
To investigate LIN28B gene variants in children with idiopathic central precocious puberty (CPP).
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