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	Missense mutations in LAMA2 causing a new phenotype of mild cognitive impairment proximal myopathy, seizure, and severe leukoencephalopathy: A case report and protein analysis
	Ding, Man; Wang, Xi; Zeng, Yanping; Lu, Zuneng; Cai, Shuang; Gao, Mingshi; Zhu, Wenhua; Luo, Sushan; Zhao, Chongbo; Xiao, Zheman
刊名	CLINICAL NEUROPATHOLOGY
	2019
卷号	38期号:3
关键词	congenital muscular dystrophy LAMA2 la minin-alpha 2-deficiency MDC1A
ISSN号	0722-5091
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/3594798
专题	复旦大学上海医学院
推荐引用方式 GB/T 7714	Ding, Man,Wang, Xi,Zeng, Yanping,et al. Missense mutations in LAMA2 causing a new phenotype of mild cognitive impairment proximal myopathy, seizure, and severe leukoencephalopathy: A case report and protein analysis[J]. CLINICAL NEUROPATHOLOGY,2019,38(3).
APA	Ding, Man.,Wang, Xi.,Zeng, Yanping.,Lu, Zuneng.,Cai, Shuang.,...&Xiao, Zheman.(2019).Missense mutations in LAMA2 causing a new phenotype of mild cognitive impairment proximal myopathy, seizure, and severe leukoencephalopathy: A case report and protein analysis.CLINICAL NEUROPATHOLOGY,38(3).
MLA	Ding, Man,et al."Missense mutations in LAMA2 causing a new phenotype of mild cognitive impairment proximal myopathy, seizure, and severe leukoencephalopathy: A case report and protein analysis".CLINICAL NEUROPATHOLOGY 38.3(2019).

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