Reading-frame restoration with an apolipoprotein B gene frameshift mutation.
We examined a mutant human apolipoprotein B (apoB) allele that causes hypobetalipoproteinemia and has a single cytosine deletion in exon 26. This frameshift mutation was associated with the synthesis of a truncated apoB protein of the predicted size; however, studies in human subjects and minigene e...
Gorde:
| Argitaratua izan da: | Proc Natl Acad Sci U S A |
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| Egile Nagusiak: | , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
National Academy of Sciences
1992
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC50565/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1454832/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.89.23.11431 |
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