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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
DOI10.1002/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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