Autosomal dominant iris hypoplasia is caused by a mutation in the rieger syndrome (rieg/pitx2) gene
Author:
Publisher
Elsevier BV
Subject
Ophthalmology
Reference5 articles.
1. Familial glaucoma in nine generations of a South Hampshire family;Martin;Br J Ophthalmol,1974
2. Linkage of autosomal dominant iris hypoplasia to the Rieger syndrome locus;Héon;Hum Mol Genet,1995
3. Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4;Murray;Nat Genet,1992
4. Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome;Semina;Nat Genet,1996
5. Genetic clues to glaucoma's secrets;Lichter;Am J Ophthalmol,1994
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