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Atypical Haemolytic Uraemic Syndrome Associated with a Hybrid Complement Gene
BACKGROUND: Sequence analysis of the regulators of complement activation (RCA) cluster of genes at chromosome position 1q32 shows evidence of several large genomic duplications. These duplications have resulted in a high degree of sequence identity between the gene for factor H (CFH) and the genes f...
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| Main Authors: | , , , , , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2006
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1626556/ https://ncbi.nlm.nih.gov/pubmed/17076561 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pmed.0030431 |
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