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Whole-exome sequencing in patients with premature ovarian insufficiency: early detection and early intervention
BACKGROUND: The loss of ovarian function in women, referred to as premature ovarian insufficiency (POI), is associated with a series of concomitant diseases. POI is genetically heterogeneous, and in most cases, the etiology is unknown. METHODS: Whole-exome sequencing (WES) was performed on DNA sampl...
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| Publicado en: | J Ovarian Res |
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| Autores principales: | , , , , , , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
BioMed Central
2020
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7510158/ https://ncbi.nlm.nih.gov/pubmed/32962729 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13048-020-00716-6 |
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