New MCM8 mutation associated with premature ovarian insufficiency and chromosomal instability in a highly consanguineous Tunisian family
Fertility and Sterility Sep 02, 2017
Bouali N, et al. – The objective of this study is to identify the gene(s) involved in the etiology of premature ovarian insufficiency in a highly consanguineous Tunisian family. These outcomes provide additional support to the view that minichromosome maintenance 8 gene (MCM8) mutations are involved in the primary ovarian insufficiency phenotype.
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