Abstract
1例主诉为间断皮肤黄染5年患儿就诊于北京儿童医院血液科,经过相关化验及基因测序检查,最终诊断为遗传性葡萄糖磷酸异构酶缺乏症。葡萄糖磷酸异构酶缺乏症临床罕见。.
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More From: Zhonghua er ke za zhi = Chinese journal of pediatrics
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