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Gene structure and chromosomal localization of mouse Opa1 : its exclusion from the Bst locus
BACKGROUND: Autosomal dominant optic atrophy type 1 (DOA) is the most common form of hereditary optic atrophy in human. We have previously identified the OPA1 gene and shown that it was mutated in patients with DOA. OPA1 is a novel member of the dynamin GTPase family that play a role in the distribu...
| Autores principales: | , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2003
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC156655/ https://www.ncbi.nlm.nih.gov/pubmed/12735796 http://dx.doi.org/10.1186/1471-2156-4-8 |