Varaico: Literature-Extracted Genetic Variants

Gene:FOXL2
Variant:p.P192delFs
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FOXL2

NM_023067.4:p.P192delFs

Associated Papers

Novel variants associated with premature ovarian insufficiency in Russian adolescents.

Tsabai P et al.

Frontiers in Endocrinology, 2025

41393291 (PubMed )
Supplement: Table1.xlsx › Supplementary_Table_2

Genetic landscape of a large cohort of Primary Ovarian Insufficiency: New genes and pathways and implications for personalized medicine.

Heddar A et al.

Ebiomedicine, 2022

36099812 (PubMed )
Supplement: mmc1.pdf

Ovarian Reserve and ART Outcomes in Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome Patients With FOXL2 Mutations.

Meng T et al.

Frontiers in Endocrinology, 2022

A new FOXL2 gene mutation in a woman with premature ovarian failure and sporadic blepharophimosis-ptosis-epicanthus inversus syndrome.

Corrêa FJ et al.

Fertility and Sterility, 2010

The human FOXL2 mutation database.

Beysen D et al.

Human Mutation, 2004

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."