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Human Molecular Genetics, 2013, Vol. 22, No. 4
DOI:10.1093/hmg/dds473
Advance Access published on November 2, 2012656667A mutation in the FAM36A gene, the human
ortholog of COX20, impairs cytochrome
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What is ortholog of cox20 impairs?
Ortholog of cox20 impairs is a gene that is similar to the cox20 gene but has a negative effect on its function.
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Researchers or scientists studying the cox20 gene and its related pathways are required to file ortholog of cox20 impairs.
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To fill out the ortholog of cox20 impairs, one would need to provide detailed information on the gene sequence, functional effects, and any experimental data supporting the impairment.
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The purpose of ortholog of cox20 impairs is to highlight genes that have a similar function to cox20 but may have detrimental effects, providing valuable insights into gene function and potential therapeutic targets.
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Information such as gene sequence, functional effects, experimental data, and potential therapeutic implications must be reported on ortholog of cox20 impairs.
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