MCM8 and MCM9 Nucleotide Variants in Women with Primary Ovarian Insufficiency | Zendy

Swapna S. Desai | Zendy; Michelle A. Wood | Zendy; Jelena Matic | Zendy; Jaqueline Chipkin | Zendy; Huaiyang Jiang | Zendy; Anne Bachelot | Zendy; Jérôme Dulon | Zendy; Cinzia Sala | Zendy; Caterina Barbieri | Zendy; Massimiliano Cocca | Zendy; Daniela Toniolo | Zendy; Touraine Philippe | Zendy; Selma F. Witchel | Zendy; Aleksandar Rajkovic | Zendy

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MCM8 and MCM9 Nucleotide Variants in Women with Primary Ovarian Insufficiency

Author(s) -

Swapna S. Desai,

Michelle A. Wood,

Jelena Matic,

Jaqueline Chipkin,

Huaiyang Jiang,

Anne Bachelot,

Jérôme Dulon,

Cinzia Sala,

Caterina Barbieri,

Massimiliano Cocca,

Daniela Toniolo,

Touraine Philippe,

Selma F. Witchel,

Aleksandar Rajkovic

Publication year - 2016

Publication title -

the journal of clinical endocrinology and metabolism

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 2.206

H-Index - 353

eISSN - 1945-7197

pISSN - 0021-972X

DOI - 10.1210/jc.2016-2565

Subject(s) - minichromosome maintenance , minichromosome , biology , dna damage , cancer research , gene , genetics , oncology , medicine , dna repair , dna , eukaryotic dna replication , genome

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).

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