Duplication as well as haploinsufficiency of the forkhead/winged-helix transcription factor FOXC1 cause human anterior segment dysgenesis.

被引：0

作者：

Mirzayans, F

Saleem, R

Gould, DB

Marshall, J

Lehmann, O

Jordan, T

Raymond, V

Mears, AJ

Walter, MA

机构：

[1] Univ Alberta, Edmonton, AB, Canada

[2] Inst Ophthalmol, Dept Mol Genet, London, England

[3] Southampton Gen Hosp, Inst Eye, Southampton SO9 4XY, Hants, England

[4] CHU Laval, Ctr Rech, Quebec City, PQ G1V 4G2, Canada

[5] Univ Laval, Quebec City, PQ, Canada

[6] Univ Michigan, Kellogg Eye Ctr, Ann Arbor, MI 48109 USA

来源：

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D O I：

暂无

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

2780

引用

页码：653 / 653

页数：1