Identification of the mutations associated with hereditary hyperferritinemia cataract syndrome and hemochromatosis in a Brazilian family

• 作者FGA Meneses; B Schnabel; IDCG Silva; FL Alberto; L Toma; HB Nader; CC Lopes
• 卷第79卷
• 期第2期
• 印刷ISSN0009-9163
• 电子ISSN1399-0004
• 文件大小592.06KB
• 发表时间2011
• DOI10.1111/j.1399-0004.2010.01517.x
• 页码189-192