急性间歇性卟啉病基因诊断研究进展(2)
[4]Susa S， Daimon M， Kato T， et al. A novel G168X mutation and a recurrent 730-731delCT mutation of the porphobilinogen deaminase gene in Japanese patients with acute intermittent porphyria. Blood Cells Mol Dis ......
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