SEC23B基因突变引起的罕见继发性血色病一例
Journal of Hepatopancreatobiliary Surgery（2023）
Abstract
血色病是人体内铁代谢异常导致血色素沉着,进而引发多器官功能障碍的一种代谢性疾病.其常见突变基因包括HAMP、HFE2、HFE、SLC40A1、TFR2等.
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