Congenital primary aphakia

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[2]. Sibel Ugur Iseri, et al. Seeing clearly: the dominant and recessive nature of FOXE3 in eye developmental anomalies. Hum Mutat. 2009 Oct;30(10):1378-86. [Content Brief]

[3]. Sophie Valleix, et al. Homozygous nonsense mutation in the FOXE3 gene as a cause of congenital primary aphakia in humans. Am J Hum Genet. 2006 Aug;79(2):358-64. [Content Brief]