Cargando…
A novel heterozygous ERCC6 variant identified in a Chinese family with non‐syndromic primary ovarian insufficiency
BACKGROUND: Premature ovarian insufficiency (POI) is a clinical syndrome occurring in women before 40 with decreased ovarian function. Up to 25% of POI cases result from genetic factors that remain largely unknown. The Excision repair cross‐complementing, group 6 (ERCC6) variant has been found to ca...
| Autores principales: | , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2022
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9544206/ https://www.ncbi.nlm.nih.gov/pubmed/35975393 http://dx.doi.org/10.1002/mgg3.2040 |