Hasil Pencarian - Min-Fei Pei
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An intron mutation in the ACVRL1 may be associated with a transcriptional regulation defect in a Chinese family with hereditary hemorrhagic telangiectasia. oleh Qian Yu, Xiao-Hui Shen, Ying Li, Rui-Juan Li, Ji Li, Yun-Ya Luo, Su-Fang Liu, Ming-Yang Deng, Min-Fei Pei, Guang-Sen Zhang
Diterbitkan 2013-01-01
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