Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
Open angle glaucoma 1M is a disease that manifests in early adulthood. Although hereditary its genetic cause is not completely discovered. Genetic localization is the 5q22.1-q32 chromosomal region.
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Wang DY et al. (2004) Absence of myocilin and optineurin mutations in a large Philippine family with juvenile onset primary open angle glaucoma. 
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| 2. |
Pang CP et al. (2006) A genome-wide scan maps a novel juvenile-onset primary open angle glaucoma locus to chromosome 5q.
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| 3. |
Fan BJ et al. (2007) Fine mapping of new glaucoma locus GLC1M and exclusion of neuregulin 2 as the causative gene.
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| 4. |
OMIM.ORG article Omim 610535
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