Genomic deletions in <it>OPA1 </it>in Danish patients with autosomal dominant optic atrophy
<p>Abstract</p> <p>Background</p> <p>Autosomal dominant optic atrophy (ADOA, Kjer disease, MIM #165500) is the most common form of hereditary optic neuropathy. Mutations in <it>OPA1 </it>located at chromosome 3q28 are the predominant cause for ADOA explainin...
| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
BMC
2011-04-01
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| Series: | BMC Medical Genetics |
| Online Access: | http://www.biomedcentral.com/1471-2350/12/49 |