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axenfeld-rieger syndrome
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PITX2
Autosomal dominant iris hypoplasia is caused by a mutation in the Rieger syndrome (RIEG/PITX2) gene
Mutation in the RIEG1 gene in patients with iridogoniodysgenesis syndrome
The molecular basis of Rieger syndrome. Analysis of Pitx2 homeodomain protein activities
Pitx2, a bicoid-type homeobox gene, is involved in a lefty-signaling pathway in determination of left-right asymmetry
FOXC1
Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly
Expression of the Mf1 gene in developing mouse hearts: implication in the development of human congenital heart defects
Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25
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multi-step regulation of transcription by pitx2
species not specified
one gene
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