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
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
Successful pregnancy after ovulation induction with human chorionic gonadotropin in a woman with selective luteinising hormone deficiency.
Sasaki LMP et al.
Human Reproduction (oxford, England), 2021
Homozygous nonsense mutation Trp28X in the LHB gene causes male hypogonadism.
Yang X et al.
Journal of Assisted Reproduction and Genetics, 2018
Inactivating mutations of luteinizing hormone beta-subunit or luteinizing hormone receptor cause oligo-amenorrhea and infertility in women.
Arnhold IJ et al.
Hormone Research, 2009
Luteinizing hormone beta mutation and hypogonadism in men and women.
Lofrano-Porto A et al.
The New England Journal of Medicine, 2007
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