Associated Papers
Genetics of Idiopathic Hypogonadotropic Hypogonadism.
Topaloğlu AK et al.
Journal of Clinical Research in Pediatric Endocrinology, 2025
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
Mechanism of female CHH caused by compound heterozygous mutations in the LHB gene.
Ma H et al.
Journal of Assisted Reproduction and Genetics, 2025
Luteinizing hormone β-subunit deficiency: Report of a novel LHB likely pathogenic variant and a systematic review of the published literature.
Barnabas R et al.
Clinical Endocrinology, 2023
Male hypogonadism caused by a homozygous missense mutation of the LHB gene.
Chen J et al.
The Korean Journal of Internal Medicine, 2021
Homozygous nonsense mutation Trp28X in the LHB gene causes male hypogonadism.
Yang X et al.
Journal of Assisted Reproduction and Genetics, 2018
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