A novel mutation of AMHR2 in two siblings with persistent Müllerian duct syndrome
Articles > Article · 2018
Authors: Edip Unal, Yusuf Kenan Haspolat, Ruken Yıldırım, Suat Tekin, Vasfiye Demir, Hüseyin Onay
Journal of Clinical Research in Pediatric Endocrinology, International, WoS, 2018, vol 10, pp 387-390
DOI: 10.4274/jcrpe.0013
Summary
gene that was identified for the first time. This presented with different phenotypes in two siblings.