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bibliographicCitation Yao K, Dai Y, Shen J, Wang Y, Yang H, Wu R, Liao Q, Wu H, Fang X, Shali S, Xu L, Hao M, Lin C, Sun Z, Liu Y, Li M, Wang Z, Gao Q, Zhang S, Li C, Gao W, Ge L, Zou Y, Sun A, Qian J, Jin L, Hong S, Zheng Y, Ge J. Exome sequencing identifies rare mutations of LDLR and QTRT1 conferring risk for early-onset coronary artery disease in Chinese. Natl Sci Rev. 2022 Aug;9(8):nwac102. PMID: 36060302; PMCID: PMC9429139.
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date 2022-05-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://pubmed.ncbi.nlm.nih.gov/PMC9429139
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language English
source https://pubmed.ncbi.nlm.nih.gov/
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title Exome sequencing identifies rare mutations of LDLR and QTRT1 conferring risk for early-onset coronary artery disease in Chinese
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