首页 | 本学科首页   官方微博 | 高级检索  
   检索      


A novel loss-of-function mutation in OTX2 in a patient with anophthalmia and isolated growth hormone deficiency
Authors:Liat Ashkenazi-Hoffnung  Yael Lebenthal  Alexander W Wyatt  Nicola K Ragge  Sumito Dateki  Maki Fukami  Tsutomu Ogata  Moshe Phillip  Galia Gat-Yablonski
Institution:(1) The Jesse Z and Sara Lea Shafer Institute of Endocrinology and Diabetes, National Center for Childhood Diabetes, Schneider Children’s Medical Center of Israel, 14 Kaplan Street, 49202 Petach Tikva, Israel;(2) Felsenstein Medical Research Center, 49202 Petah Tikva, Israel;(3) Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel;(4) Department of Physiology, Anatomy and Genetics, University of Oxford, Le Gros Clark Building, Oxford, OX1 3QX, UK;(5) Moorfields Eye Hospital NHS Foundation Trust, London, EC1V 2PD, UK;(6) Department of Endocrinology and Metabolism, National Research Institute for Child Health and Development, Tokyo, Japan;(7) Department of Pediatrics, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan;
Abstract:
Keywords:
本文献已被 SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号