A Novel Homozygous Missense < b > < i > FSHR < /i > < /b > Variant Associated with Hypergonadotropic Hypogonadism in Two Siblings from a Brazilian Family

In conclusion, the novel homozygousFSHR variant observed in 2 siblings with HH can expand the spectrum ofFSHRmutations in humans.Sex Dev
Source: Sexual Development - Category: Biology Source Type: research