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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Detalles Bibliográficos
Autores principales: Jin, Haengun, Ahn, JuWon, Park, YoungJoon, Sim, JeongMin, Park, Han Sung, Ryu, Chang Soo, Kim, Nam Keun, Kwack, KyuBum
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7590468/
https://www.ncbi.nlm.nih.gov/pubmed/33109206
http://dx.doi.org/10.1186/s12920-020-00813-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7590468/
https://www.ncbi.nlm.nih.gov/pubmed/33109206
http://dx.doi.org/10.1186/s12920-020-00813-x

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