Homozygous loss-of-function mutations in SOHLH1 in patients with nonsyndromic hypergonadotropic hypogonadism


Bayram Y., Bayram Y., Gulsuner S., Gulsuner S., GÜRAN T., Guran T., ...Daha Fazla

Journal of Clinical Endocrinology and Metabolism, cilt.100, sa.5, 2015 (SCI-Expanded) identifier identifier identifier