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	De novo mutations in GRIN1 cause extensive bilateral polymicrogyria
	Fry, Andrew E.*; Fawcett, Katherine A.; Zelnik, Nathanel; Yuan, Hongjie; Thompson, Belinda A. N.; Shemer-Meiri, Lilach; Cushion, Thomas D.; Mugalaasi, Hood; Sims, David; Stoodley, Neil
刊名	Brain
	2018
卷号	141期号:3页码:698-712
关键词	GRIN1 GluN1 N -methyl- d -aspartate receptor NR1 Polymicrogyria
ISSN号	0006-8950
DOI	10.1093/brain/awx358
URL标识	查看原文
WOS记录号	WOS:000426813600017
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/3339651
专题	中南大学
作者单位	1.[Mugalaasi, Hood 2.Fry, Andrew E.] Univ Wales Hosp, Inst Med Genet, Heath Pk, Cardiff CF14 4XW, S Glam, Wales.
推荐引用方式 GB/T 7714	Fry, Andrew E.*,Fawcett, Katherine A.,Zelnik, Nathanel,et al. De novo mutations in GRIN1 cause extensive bilateral polymicrogyria[J]. Brain,2018,141(3):698-712.
APA	Fry, Andrew E.*.,Fawcett, Katherine A..,Zelnik, Nathanel.,Yuan, Hongjie.,Thompson, Belinda A. N..,...&Pilz, Daniela T..(2018).De novo mutations in GRIN1 cause extensive bilateral polymicrogyria.Brain,141(3),698-712.
MLA	Fry, Andrew E.*,et al."De novo mutations in GRIN1 cause extensive bilateral polymicrogyria".Brain 141.3(2018):698-712.

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