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Genome-wide methylation study of whole blood cells DNA in men with congenital hypopituitarism disease
Congenital hypopituitarism (CH) is a relatively rare disease that is characterized by the deficiency of one or more hormones secreted by the pituitary gland, which leads to metabolic disorders, amenorrhea and infertility. However, the underlying molecular mechanisms of CH have not yet been fully elu...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257856/ https://www.ncbi.nlm.nih.gov/pubmed/30365064 http://dx.doi.org/10.3892/ijmm.2018.3945 |