Novelmutation相关论文
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Identification of a Novel Mutation in Solute Carrier Family 29, Member 3 in a Chinese Patient with H
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目的 研究黏多糖贮积症ⅣA型(mucopolysaccharidosis type ⅣA,MPS ⅣA)患者发病的分子遗传学机制,揭示其基因型与表现型的相互关......
