Varaico: Literature-Extracted Genetic Variants

Gene:MEIOB
Variant:p.S366fs
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MEIOB

NM_001163560.3:p.S366fs

Associated Papers

Summarizing the human genes and their variants causative of non-obstructive azoospermia uncovered using whole genome/exome sequencing.

Ibrahim R et al.

Reproductive Biology, 2025

Novel MEIOB pathogenic variants including a homozygous non-canonical splicing variant, cause meiotic arrest and human non-obstructive azoospermia.

Zhu X et al.

Clinical Genetics, 2024

Genetic variants underlying spermatogenic arrests in men with non-obstructive azoospermia.

Ozturk S

Cell Cycle (georgetown, Tex.), 2023

Novel MEIOB variants cause primary ovarian insufficiency and non-obstructive azoospermia.

Wang Y et al.

Frontiers in Genetics, 2022

Shared genetics between nonobstructive azoospermia and primary ovarian insufficiency.

Verrilli L et al.

F&s Reviews, 2021

A new MEIOB mutation is a recurrent cause for azoospermia and testicular meiotic arrest.

Gershoni M et al.

Human Reproduction (oxford, England), 2019

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