A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start site

• 作者Kathryn P. Burdon; Shiwani Sharma; Celia S. Chen; David P. Dimasi; David A. Mackey; Jamie E. Craig
• 卷第28卷
• 期第7期
• 印刷ISSN1059-7794
• 电子ISSN1098-1004
• 文件大小469.25KB
• 发表时间2007
• DOI10.1002/humu.9501
• 页码742-742