Cargando…
Novel loss‐of‐function mutation in MCM8 causes premature ovarian insufficiency
BACKGROUND: Premature ovarian insufficiency (POI) is one major cause of female infertility, minichromosome maintenance complex component 8 (MCM8) has been reported to be responsible for POI. METHODS: Whole‐exome sequencing was performed to identify the genetic variants of women with POI. Sanger sequ...
Autores principales: | Zhang, Ya‐Xin, He, Wen‐Bin, Xiao, Wen‐Juan, Meng, Lan‐Lan, Tan, Chen, Du, Juan, Lu, Guang‐Xiu, Lin, Ge, Tan, Yue‐Qiu |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7196458/ https://www.ncbi.nlm.nih.gov/pubmed/32048466 http://dx.doi.org/10.1002/mgg3.1165 |
Ejemplares similares
-
In-Frame Variants in STAG3 Gene Cause Premature Ovarian Insufficiency
por: Xiao, Wen-Juan, et al.
Publicado: (2019) -
Homozygous variants in SYCP2L cause premature ovarian insufficiency
por: He, Wen-Bin, et al.
Publicado: (2021) -
Novel FOXL2 mutations cause blepharophimosis‐ptosis‐epicanthus inversus syndrome with premature ovarian insufficiency
por: Yang, Xiao‐Wen, et al.
Publicado: (2018) -
The Role of MCM9 in the Etiology of Sertoli Cell-Only Syndrome and Premature Ovarian Insufficiency
por: Potorac, Iulia, et al.
Publicado: (2023) -
Novel MEIOB variants cause primary ovarian insufficiency and non-obstructive azoospermia
por: Wang, Yurong, et al.
Publicado: (2022)