Deletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin alpha 2-related muscular dystrophy | |
Ge, Lin; Liu, Aijie; Gao, Kai; Du, Renqian; Ding, Juan; Mao, Bing; Hua, Ying; Zhang, Xiaoli; Tan, Dandan; Yang, Haipo | |
刊名 | SCIENTIFIC REPORTS |
2018 | |
卷号 | 8 |
ISSN号 | 2045-2322 |
URL标识 | 查看原文 |
语种 | 英语 |
内容类型 | 期刊论文 |
URI标识 | http://www.corc.org.cn/handle/1471x/3604311 |
专题 | 复旦大学上海医学院 |
推荐引用方式 GB/T 7714 | Ge, Lin,Liu, Aijie,Gao, Kai,et al. Deletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin alpha 2-related muscular dystrophy[J]. SCIENTIFIC REPORTS,2018,8. |
APA | Ge, Lin.,Liu, Aijie.,Gao, Kai.,Du, Renqian.,Ding, Juan.,...&Xiong, Hui.(2018).Deletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin alpha 2-related muscular dystrophy.SCIENTIFIC REPORTS,8. |
MLA | Ge, Lin,et al."Deletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin alpha 2-related muscular dystrophy".SCIENTIFIC REPORTS 8(2018). |
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