• PMID: 9624193
• Gene Name: FSHB
• Condition: Male hypogonadism
• Association: The study reports a case of secondary hypogonadism associated with an isolated deficiency of follicle-stimulating hormone in a young man.
• Mutation: deletion of the second and third nucleotides (thymidine and guanine) in codon 61
• Population size: 3
• Population details: 3 (1 male hypogonadism)
• Sex: Male
• Infertility type: Male infertility
• Other associated phenotypes: Male infertility

Male hypogonadism due to a mutation in the gene for the beta-subunit of follicle-stimulating hormone

Phillip M, Arbelle JE, Segev Y, Parvari R.

No abstract available