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Identification of potential causal variants for premature ovarian failure by whole exome sequencing
BACKGROUND: Premature ovarian failure (POF) is a highly heterogeneous disorder that occurs in 1% of women of reproductive age. Very few causative genes and variants contributing to POF have been detected, and the disease remains incompletely understood. In this study, we used whole exome sequencing...
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| Publicat a: | BMC Med Genomics |
|---|---|
| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7590468/ https://ncbi.nlm.nih.gov/pubmed/33109206 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-020-00813-x |
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