Genetic insights into the complexity of premature ovarian insufficiency
Abstract Premature Ovarian Insufficiency (POI) is a highly heterogeneous condition characterized by ovarian dysfunction in women occurring before the age of 40, representing a significant cause of female infertility. It manifests through primary or secondary amenorrhea. While more than half of POI c...
Saved in:
Main Authors: | Linhang Nie (Author), Xiaojie Wang (Author), Songyuan Wang (Author), Zhidan Hong (Author), Mei Wang (Author) |
---|---|
Format: | Book |
Published: |
BMC,
2024-08-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
DNA double-strand break genetic variants in patients with premature ovarian insufficiency
by: Xuechun Ding, et al.
Published: (2023) -
Explaining the unexplained: new genetic mutations in unexplained premature ovarian insufficiency
by: Anna K. Knight, Ph.D
Published: (2020) -
Plasma metabolomic characterization of premature ovarian insufficiency
by: Xing-Yu Zhou, et al.
Published: (2023) -
Premature ovarian insufficiency in patients with galactosemia
by: Irina V. Karachentsova, et al.
Published: (2024) -
Premature ovarian insufficiency - to treat or not to treat?
by: O. S. Zahorodnia, et al.
Published: (2019)