Analbuminemia: three cases resulting from different point mutations in the albumin gene.
Analbuminemia is a very rare recessive disorder in which subjects have little or no circulating albumin, although albumin is normally the most abundant plasma protein and has many functions. Analbuminemia is caused by a variety of mutations in the albumin gene and is exhibited only by subjects homoz...
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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
1994
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC44823/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7937781/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.91.20.9417 |
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