Alu-mediated inactivation of the human CMP- N-acetylneuraminic acid hydroxylase gene
Inactivation of the CMP-N-acetylneuraminic acid hydroxylase gene has provided an example of human-specific genomic mutation that results in a widespread biochemical difference between human and nonhuman primates. We have found that, although a region containing a 92-bp exon and an AluSq element in t...
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| Publicado no: | Proc Natl Acad Sci U S A |
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| Principais autores: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
National Academy of Sciences
2001
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC58741/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/11562455/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.191268198 |
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