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Impaired dimer assembly and decreased stability of naturally recurring R260C mutant A subunit for coagulation factor XIII
Factor XIII (FXIII) consists of catalytic A subunits (FXIII-A) and carrier B subunits. Congenital FXIII deficiency is a severe bleeding disorder. We previously identified an R260C missense mutation and an exon-IV deletion in Japanese patients’ F13A genes. To characterize the molecular basis of this...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3619964/ https://ncbi.nlm.nih.gov/pubmed/22923741 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/jb/mvs088 |
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