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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Detalles Bibliográficos
Autores principales: Liu, Hongli, Wei, Xiaoli, Sha, Yanwei, Liu, Wensheng, Gao, Haijie, Lin, Jin, Li, Youzhu, Tang, Yaling, Wang, Yifeng, Wang, Yanlong, Su, Zhiying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7510158/
https://www.ncbi.nlm.nih.gov/pubmed/32962729
http://dx.doi.org/10.1186/s13048-020-00716-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7510158/
https://www.ncbi.nlm.nih.gov/pubmed/32962729
http://dx.doi.org/10.1186/s13048-020-00716-6

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