TBX6 missense variants expand the mutational spectrum in a non-Mendelian inheritance disease | |
Chen Weisheng; Lin Jiachen; Wang Lianlei; Li Xiaoxin; Zhao Sen; Liu Jiaqi; Akdemir Zeynep C; Zhao Yanxue; Du Renqian; Ye Yongyu | |
2019 | |
关键词 | TBX6 gene compound inheritance model congenital scoliosis (CS) gene dosage genotype-phenotype correlation |
ISSN号 | 1098-1004 |
DOI | 10.1002/humu.23907 |
URL标识 | 查看原文 |
收录类别 | PUBMED |
内容类型 | 期刊论文 |
URI标识 | http://www.corc.org.cn/handle/1471x/6338674 |
专题 | 中国医学科学院 北京协和医学院 |
推荐引用方式 GB/T 7714 | Chen Weisheng,Lin Jiachen,Wang Lianlei,et al. TBX6 missense variants expand the mutational spectrum in a non-Mendelian inheritance disease[J],2019. |
APA | Chen Weisheng.,Lin Jiachen.,Wang Lianlei.,Li Xiaoxin.,Zhao Sen.,...&Wu Nan.(2019).TBX6 missense variants expand the mutational spectrum in a non-Mendelian inheritance disease.. |
MLA | Chen Weisheng,et al."TBX6 missense variants expand the mutational spectrum in a non-Mendelian inheritance disease".(2019). |
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