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Ito YA 1
Showing records 1 to 1 | Display all abstracts from Ito YA24008 Severe molecular defects of a novel FOXC1 W152G mutation result in aniridia
Ito YA; Footz TK; Berry FB; Mirzayans F; Yu M; Khan AO; Walter MA
Investigative Ophthalmology and Visual Science 2009; 50: 3573-3579
