Identification of novel KIF11 mutations in patients with familial exudative vitreoretinopathy and a phenotypic analysis
出版年份 2016 全文链接
标题
Identification of novel KIF11 mutations in patients with familial exudative vitreoretinopathy and a phenotypic analysis
作者
关键词
-
出版物
Scientific Reports
Volume 6, Issue 1, Pages -
出版商
Springer Nature
发表日期
2016-05-24
DOI
10.1038/srep26564
参考文献
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- Mutations in KIF11 Cause Autosomal-Dominant Microcephaly Variably Associated with Congenital Lymphedema and Chorioretinopathy
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- A novelKIF11mutation in a Turkish patient with microcephaly, lymphedema, and chorioretinal dysplasia from a consanguineous family
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