Screening for mutations in selected miRNA genes in hypogonadotropic hypogonadism patients.

Iivonen, Anna-Pauliina; Känsäkoski, Johanna; Vaaralahti, Kirsi; Raivio, Taneli

Iivonen, Anna-Pauliina; Känsäkoski, Johanna; Vaaralahti, Kirsi; Raivio, Taneli.

Afiliação

Iivonen AP; Institute of Biomedicine/Physiology, Biomedicum Helsinki and Stem Cells and Metabolism Research Program, University of Helsinki, Helsinki, Finland.
Känsäkoski J; Institute of Biomedicine/Physiology, Biomedicum Helsinki and Stem Cells and Metabolism Research Program, University of Helsinki, Helsinki, Finland.
Vaaralahti K; Institute of Biomedicine/Physiology, Biomedicum Helsinki and Stem Cells and Metabolism Research Program, University of Helsinki, Helsinki, Finland.
Raivio T; Institute of Biomedicine/Physiology, Biomedicum Helsinki and Stem Cells and Metabolism Research Program, University of Helsinki, Helsinki, Finland.

Endocr Connect ; 8(5): 506-509, 2019 May 01.

Article em En | MEDLINE | ID: mdl-30999277

Palavras-chave

Kallmann syndrome; hypogonadotropic hypogonadism; microRNA; mutation

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Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Prognostic_studies / Screening_studies Idioma: En Revista: Endocr Connect Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Finlândia

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