A case report: a heterozygous deletion (2791_2805 del) in exon 18 of the filamin C gene causing filamin C-related myofibrillar myopathies in a Chinese family | |
Miao, Jing; Su, Fei-fei; Liu, Xue-mei; Wei, Xiao-jing; Yuan, Yun; Yu, Xue-fan | |
刊名 | BMC NEUROLOGY |
2018 | |
卷号 | 18 |
关键词 | Deletion Filamin C gene Dominant Myofibrillar myopathy Case report |
ISSN号 | 1471-2377 |
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/3535369 |
专题 | 吉林大学白求恩第一医院 |
推荐引用方式 GB/T 7714 | Miao, Jing,Su, Fei-fei,Liu, Xue-mei,et al. A case report: a heterozygous deletion (2791_2805 del) in exon 18 of the filamin C gene causing filamin C-related myofibrillar myopathies in a Chinese family[J]. BMC NEUROLOGY,2018,18. |
APA | Miao, Jing,Su, Fei-fei,Liu, Xue-mei,Wei, Xiao-jing,Yuan, Yun,&Yu, Xue-fan.(2018).A case report: a heterozygous deletion (2791_2805 del) in exon 18 of the filamin C gene causing filamin C-related myofibrillar myopathies in a Chinese family.BMC NEUROLOGY,18. |
MLA | Miao, Jing,et al."A case report: a heterozygous deletion (2791_2805 del) in exon 18 of the filamin C gene causing filamin C-related myofibrillar myopathies in a Chinese family".BMC NEUROLOGY 18(2018). |
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