首页 | 本学科首页   官方微博 | 高级检索  
     


Richner-Hanhart syndrome: report of a case with a novel mutation of tyrosine aminotransferase
Authors:Minami-Hori M  Ishida-Yamamoto A  Katoh N  Takahashi H  Iizuka H
Affiliation:1. Department of Dermatology, Asahikawa Medical College, Midorigaoka Higashi 2-1-1-1, Asahikawa 078-8510, Japan;2. Department of Dermatology, Wakkanai General Hospital, 4-Chome Chuou, Wakkanai 097-0021, Japan;1. Department of Cardiology, Government Medical College, Trivandrum, Kerala, India;2. P. D. Hinduja Hospital and MRC, Mumbai, Maharashtra, India;1. Department of Pediatrics, Hacettepe University Ihsan Doğramacı Childrens Hospital, Ankara, Turkey;2. Division of Immunology, Hacettepe University Ihsan Doğramacı Childrens Hospital, Ankara, Turkey;3. Division of Hematology, Hacettepe University Ihsan Doğramacı Childrens Hospital, Ankara, Turkey;4. NSERM U768, Hôpital Necker Enfants Malades, Paris, France;1. División de Genética, Centro de Investigación Biomédica de Occidente, Instituto Mexicano del Seguro Social, Guadalajara, Jalisco, México;2. Doctorado en Genética Humana, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Guadalajara, Jalisco, México;3. Facultad de Medicina, Universidad Autónoma de Guadalajara, Guadalajara, Jalisco, México
Abstract:
Keywords:
本文献已被 ScienceDirect PubMed 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