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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:J Ovarian Res
Autors principals: Liu, Hongli, Wei, Xiaoli, Sha, Yanwei, Liu, Wensheng, Gao, Haijie, Lin, Jin, Li, Youzhu, Tang, Yaling, Wang, Yifeng, Wang, Yanlong, Su, Zhiying
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2020
Matèries:
Research
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars