×
Entrez Id:
3972
Gene Symbol:
LHB
LHB
0.350
GeneticVariation
disease
BEFREE
We identified a novel mutation in the LHB gene in a male patient with hypogonadism and provided evidence that LHB nonsense mutation can cause selective LH deficiency.
29476300
2018
×
Entrez Id:
3972
Gene Symbol:
LHB
LHB
0.350
GeneticVariation
disease
BEFREE
Inactivating Luteinizing hormone beta (LHB ) gene mutations are exceptionally rare and lead to hypogonadism that is particularly severe in males.
27656125
2016
×
Entrez Id:
3972
Gene Symbol:
LHB
LHB
0.350
GeneticVariation
disease
BEFREE
Hypogonadism in a patient with two novel mutations of the luteinizing hormone β-subunit gene expressed in a compound heterozygous form.
22723313
2012
×
Entrez Id:
3972
Gene Symbol:
LHB
LHB
0.350
Therapeutic
disease
CTD_human
Cryptic 17q22 deletion in a boy with a t(10;17)(p15.3;q22) translocation, multiple synostosis syndrome 1, and hypogonadotropic hypogonadism.
18449926
2008
×
Entrez Id:
3972
Gene Symbol:
LHB
LHB
0.350
Biomarker
disease
CTD_human
Cryptic 17q22 deletion in a boy with a t(10;17)(p15.3;q22) translocation, multiple synostosis syndrome 1, and hypogonadotropic hypogonadism.
18449926
2008
×
Entrez Id:
3972
Gene Symbol:
LHB
LHB
0.350
GeneticVariation
disease
BEFREE
Selective luteinizing hormone deficiency due to mutations in the luteinizing hormone beta-subunit gene (LHB) is a rare cause of hypogonadism .
17761593
2007
×
Entrez Id:
3972
Gene Symbol:
LHB
LHB
0.350
Biomarker
disease
CTD_human
Hypogonadism in a patient with a mutation in the luteinizing hormone beta-subunit gene.
15602022
2004
×
Entrez Id:
3972
Gene Symbol:
LHB
LHB
0.350
GeneticVariation
disease
BEFREE
Hypogonadism in a patient with a mutation in the luteinizing hormone beta-subunit gene.
15602022
2004
×
Entrez Id:
3972
Gene Symbol:
LHB
LHB
0.350
Therapeutic
disease
CTD_human
Hypogonadism in a patient with a mutation in the luteinizing hormone beta-subunit gene.
15602022
2004
×
Entrez Id:
3972
Gene Symbol:
LHB
LHB
0.350
Biomarker
disease
CTD_human
Failure of combined follicle-stimulating hormone-testosterone administration to initiate and/or maintain spermatogenesis in men with hypogonadotropic hypogonadism.
8263139
1993
×
Entrez Id:
3972
Gene Symbol:
LHB
LHB
0.350
Therapeutic
disease
CTD_human
Failure of combined follicle-stimulating hormone-testosterone administration to initiate and/or maintain spermatogenesis in men with hypogonadotropic hypogonadism.
8263139
1993
×
Entrez Id:
3972
Gene Symbol:
LHB
LHB
0.350
Therapeutic
disease
CTD_human
Hypogonadism caused by a single amino acid substitution in the beta subunit of luteinizing hormone.
1727547
1992
×
Entrez Id:
3972
Gene Symbol:
LHB
LHB
0.350
Biomarker
disease
CTD_human
Hypogonadism caused by a single amino acid substitution in the beta subunit of luteinizing hormone.
1727547
1992