Heterozygous FMN2 missense variant found in a family case of premature ovarian insufficiency

BACKGROUND: Premature ovarian insufficiency (POI) plagues 1% of women under 40, while quite a few remain an unknown cause. The development of sequencing has helped find pathogenic genes and reveal the relationship between DNA repair and ovarian reserve. Through the exome sequencing, our study target...

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Detalles Bibliográficos
Autores principales: Li, Jie, Peng, Tianliu, Wang, Le, Long, Panpan, Quan, Ruping, Tan, Hangjing, Zeng, Minghua, Wu, Xue, Yang, Junting, Xiao, Hongmei, Shi, Xiaobo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8886936/
https://www.ncbi.nlm.nih.gov/pubmed/35227295
http://dx.doi.org/10.1186/s13048-022-00960-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8886936/
https://www.ncbi.nlm.nih.gov/pubmed/35227295
http://dx.doi.org/10.1186/s13048-022-00960-y

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