Weimin Zhou
2PUBLICATIONS
0CO-AUTHORS
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Publications (2)
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|Dec 23, 2018
Exome sequencing reveals a de novo PRKG1 mutation in a sporadic patient with aortic dissection.Wenwen Zhang, Qian Han, Zhao Liu
|Jan 31, 2018
Whole exome sequencing reveals a stop-gain mutation of PKD2 in an autosomal dominant polycystic kidney disease family complicated with aortic dissection.Wenwen Zhang, Qian Han, Zhao Liu
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