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Case report of a novel PCDH19 frameshift mutation in a girl with epilepsy and mental retardation limited to females
Zhang, Xinying; Chen, Na; Ma, Aihua; Wang, Xueyu; Sun, Wenxiu; Gao, Yuxing
刊名MEDICINE
2018
卷号97期号:51
关键词c.2468delT epilepsy with mental retardation limited to females frameshift mutation protocadherin 19
DOI10.1097/MD.0000000000013749
URL标识查看原文
公开日期[db:dc_date_available]
内容类型期刊论文
URI标识http://www.corc.org.cn/handle/1471x/4575065
专题山东大学
作者单位Shandong Univ, Shandong Prov Hosp, Dept Pediat Neurol, Jinan, Shandong, P
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GB/T 7714
Zhang, Xinying,Chen, Na,Ma, Aihua,et al. Case report of a novel PCDH19 frameshift mutation in a girl with epilepsy and mental retardation limited to females[J]. MEDICINE,2018,97(51).
APA Zhang, Xinying,Chen, Na,Ma, Aihua,Wang, Xueyu,Sun, Wenxiu,&Gao, Yuxing.(2018).Case report of a novel PCDH19 frameshift mutation in a girl with epilepsy and mental retardation limited to females.MEDICINE,97(51).
MLA Zhang, Xinying,et al."Case report of a novel PCDH19 frameshift mutation in a girl with epilepsy and mental retardation limited to females".MEDICINE 97.51(2018).
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