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Molecular Basis of Congenital Factor XIII Deficiency in Iran
Factor XIII deficiency (FXIIID) is an extremely rare autosomal recessive disorder that has the highest incidence in Iran. The FXIIID is primarily due to mutations in the FXIII-A gene, most of which are unique. In the current study, we report all identified mutations among Iranian patients. Among 483...
Guardado en:
| Publicado en: | Clin Appl Thromb Hemost |
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| Autores principales: | , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
SAGE Publications
2016
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6714674/ https://ncbi.nlm.nih.gov/pubmed/27879471 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1076029616680473 |
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