Associated Papers
Reclassifying NOBOX variants in primary ovarian insufficiency cases with a corrected gene model and a novel quantitative framework.
Veitia RA et al.
Human Reproduction (oxford, England), 2025
40246288 (PubMed )
Supplement: deaf058_supplementary_table_s2.docx
NOBOX is a strong autosomal candidate gene in Tunisian patients with primary ovarian insufficiency.
Bouali N et al.
Clinical Genetics, 2016
Aetiological coding sequence variants in non-syndromic premature ovarian failure: From genetic linkage analysis to next generation sequencing.
Laissue P
Molecular and Cellular Endocrinology, 2015
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