Homozygous truncating mutation of the KBP gene, encoding a KIF1B-binding protein, in a familial case of fetal polymicrogyria
出版年份 2013 全文链接
标题
Homozygous truncating mutation of the KBP gene, encoding a KIF1B-binding protein, in a familial case of fetal polymicrogyria
作者
关键词
Polymicrogyria, Kinesin binding protein, Prenatal diagnosis, <em class=EmphasisTypeItalic >KBP</em> gene
出版物
NEUROGENETICS
Volume 14, Issue 3-4, Pages 215-224
出版商
Springer Nature
发表日期
2013-09-26
DOI
10.1007/s10048-013-0373-x
参考文献
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