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

被引：0
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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：
AMERICAN JOURNAL OF HUMAN GENETICS | 2001年 / 69卷 / 04期
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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
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收藏
页码：653 / 653
页数：1
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