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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...

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Detalles Bibliográficos
Autores principales: Delettre, Cécile, Lenaers, Guy, Belenguer, Pascale, Hamel, Christian P
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2003
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