Gene structure and chromosomal localization of mouse <it>Opa1 </it>: its exclusion from the Bst locus
<p>Abstract</p> <p>Background</p> <p>Autosomal dominant optic atrophy type 1 (DOA) is the most common form of hereditary optic atrophy in human. We have previously identified the <it>OPA1 </it>gene and shown that it was mutated in patients with DOA. OPA1 is...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
BMC
2003-05-01
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| Series: | BMC Genetics |
| Online Access: | http://www.biomedcentral.com/1471-2156/4/8 |