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9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia (3)

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25409 Axenfeld-Rieger syndrome and spectrum of PITX2 and FOXC1 mutations
Tumer Z; Bach-Holm D
European Journal of Human Genetics 2009; 17: 1527-1539

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25274 Human PRKC apoptosis WT1 regulator is a novel PITX2-interacting protein that regulates PITX2 transcriptional activity in ocular cells
Acharya M; Lingenfelter D J; Huang L; Gage P J; Walter M A
Journal of Biological Chemistry 2009; 284: 34829-34838

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25206 Vitreoretinal dysplasia masquerading as Peters' anomaly
Martinet V; Dureau P; Bergès O; Caputo G
European Journal of Ophthalmology 2010; 20: 228-230

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