Screening for mutations in selected miRNA genes in hypogonadotropic hypogonadism patients
In approximately half of congenital hypogonadotropic hypogonadism (cHH) patients, the genetic cause remains unidentified. Since the lack of certain mi RNAs in animal models has led to cHH, we sequenced human miRNAs predicted to regulate cHH-related genes (MIR7-3, MIR141, MIR429 and MIR200A-C) in 24...
Main Authors: | , , , |
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Format: | Article |
Language: | English |
Published: |
Bioscientifica
2019-04-01
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Series: | Endocrine Connections |
Subjects: | |
Online Access: | https://ec.bioscientifica.com/view/journals/ec/8/5/EC-19-0080.xml |