Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
Open angle glaucoma 1P is a disease that manifests in early adulthood. Although hereditary its genetic cause is not completely discovered. Genetic localization is the 12q14 chromosomal region.
| 1. |
Bennett SR et al. (1989) An autosomal dominant form of low-tension glaucoma. 
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| 2. |
None (1961) Pseudoglaucoma of autosomal, dominant inheritance. A report on three families.
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| 3. |
Fingert JH et al. (2011) Copy number variations on chromosome 12q14 in patients with normal tension glaucoma.
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| 4. |
Kawase K et al. (2012) Confirmation of TBK1 duplication in normal tension glaucoma.
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| 5. |
Fingert JH et al. (2014) TBK1 and flanking genes in human retina.
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| 6. |
Awadalla MS et al. (2015) Copy number variations of TBK1 in Australian patients with primary open-angle glaucoma.
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| 7. |
OMIM.ORG article Omim 177700
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