Rieger syndrome is not associated with PAX6 deletion: A correction to Acta Ophthalmol Scand 2001: 79: 201-203

Acta Ophthalmologica

Volumn 87, Issue 8, 2009, Pages 923-

  Riise, Ruth ^a   D'Haene, Barbara ^b   De Baere, Elfride ^b   Grønskov, Karen ^c   Brøndum Nielsen, Karen ^c  

^a OSLO UNIVERSITY HOSPITAL   (Norway)

^b GHENT UNIVERSITY HOSPITAL   (Belgium)

^c Kennedy Centre   (Denmark)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR PAX6;

AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 11; CHROMOSOME DELETION; DIAGNOSTIC ERROR; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; HUMAN; LETTER; MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; PRIORITY JOURNAL; RIEGER SYNDROME;

ABNORMALITIES, MULTIPLE; ANTERIOR EYE SEGMENT; EYE ABNORMALITIES; EYE PROTEINS; FACE; GENE DELETION; GENES, DOMINANT; HOMEODOMAIN PROTEINS; HUMANS; IRIS; PAIRED BOX TRANSCRIPTION FACTORS; REPRESSOR PROTEINS; SKIN ABNORMALITIES; SYNDROME; TOOTH ABNORMALITIES;

EID: 73349120245     PISSN: 1755375X     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1755-3768.2009.01696.x     Document Type: Letter

References (4)

1. Borges AS, Susanna R Jr., Carani JC, Betinjane AJ, Alward WL, Stone EM, Sheffield VC Nishimura DY (2002 Genetic analysis of PITX2 and FOXC1 in Rieger syndrome patients from Brazil. J Glaucoma 11 : 51 56.
2. Riise R (2005 Rieger Syndrome and PAX6 deletion. In : Amendt BA (ed.). The Molecular Mechanisms of Axenfeld-Rieger Syndrome. Georgetown : Landes Bioscience, 26 31.
3. Riise R, Storhaug K Brøndum-Nielsen K (2001 Rieger syndrome is associated with PAX6 deletion. Acta Ophthalmol Scand 79 : 201 203.
4. Semina EV, Reiter R, Leysens NJ et al. (1996 Cloning and characterization of a novel bicoid-related homeobox transcription factor, Rieg, involved in Rieger syndrome. Nat Genet 14 : 392 399.