Severe Molecular Defects of a NovelFOXC1 W152GMutation Result in Aniridia
Investigative Ophthalmology & Visual Science2009Vol. 50(8), pp. 3573–3573
Citations Over TimeTop 19% of 2009 papers
Yoko Itō, Tim Footz, Fred B. Berry, Farideh Mirzayans, May Mei-Yung Yu, Arif O. Khan, Michael A. Walter
Abstract
Severe molecular consequences, including the inability of the W152G protein aggregates to form protective aggresomes, may underlie the aniridia phenotype that results from the FOXC1 W152G mutation.
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