A review of primary hereditary optic neuropathies
Author:
Affiliation:
1. ; Department of Molecular Genetics; Institute of Ophthalmology; London
2. ; Moorfields Eye Hospital; London UK
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1024441302074/fullpdf
Reference122 articles.
1. OPAl, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28;Alexander;Nature Genetics,2000
2. Type III 3-methylglutaconic aciduria (optic atrophy plus syndrome, or Costeff optic atrophy syndrome): identification of the OPA3 gene and its founder mutation in Iraqi Jews;Anikster;Am J Hum Genet,2001
3. A gene for X-linked optic atrophy is closely linked to the Xpl 1.4Xpl 1.2 region of the X chromosome;Assink;Am J Hum Genet,1997
4. A major marker for normal tension glaucoma: association with polymorphisms in the OPAl gene;Aung;Hum Genet,2002
5. Investigating the association between OPAl polymorphisms and glaucoma: comparison between normal tension and high tension primary open angle glaucoma;Aung;Hum Genet,2002
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