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A novel TGFBR2 gene mutation of type 2 Marfan syndrome in a Chinese family

A novel TGFBR2 gene mutation of type 2 Marfan syndrome in a Chinese family
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摘要 Objective To report the clinical features and the screening Results of the pathogenic gene in type 2 Marfan syndrome patients,and the relationship between the transmembrane domain of TGFBR2 gene and the clinical phenotype.Methods The FBN1 and TGFBR2 genes were sequenced in the genomic DNA by Sanger sequence of type 2 Marfan syndrome pedigrees,and the protein structure prediction and genotype phenotypic analysis of the TGFBR2 gene transmembrane domain termination mutation were carried out.
出处 《中国循环杂志》 CSCD 北大核心 2018年第S01期124-125,共2页 Chinese Circulation Journal
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