MCM8 and MCM9 Nucleotide Variants in Women With Primary Ovarian Insufficiency

OBJECTIVE: To assess the frequency of variants, including biallelic pathogenic variants, in minichromosome maintenance 8 (MCM8) and minichromosome maintenance 9 (MCM9), other genes related to MCM8–MCM9, and DNA damage repair (DDR) pathway in participants with primary ovarian insufficiency (POI). DES...

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Vydáno v:J Clin Endocrinol Metab
Hlavní autoři: Desai, Swapna, Wood-Trageser, Michelle, Matic, Jelena, Chipkin, Jaqueline, Jiang, Huaiyang, Bachelot, Anne, Dulon, Jerome, Sala, Cinzia, Barbieri, Caterina, Cocca, Massimiliano, Toniolo, Daniela, Touraine, Philippe, Witchel, Selma, Rajkovic, Aleksandar
Médium: Artigo
Jazyk:Inglês
Vydáno: Endocrine Society 2016
Témata:
Clinical Research Articles
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5413161/
https://ncbi.nlm.nih.gov/pubmed/27802094
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2016-2565
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