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Analysis of reported SCO2 gene mutations affecting cytochrome c oxidase activity in various diseases
A large number of mutations have been reported in SCO2 (synthesis of cytochrome c oxidase) gene in association with COX deficiency reported in different diseases such as cardioencephalomyopathy, cardiomyopathy and Leigh syndrome. However, very few of these mutations have been functionally analyzed.S...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Biomedical Informatics
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4110422/ https://ncbi.nlm.nih.gov/pubmed/25097374 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.6026/97320630010329 |
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