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Clinical features of patients with homozygous complement C4A or C4B deficiency
INTRODUCTION: Homozygous deficiencies of complement C4A or C4B are detected in 1–10% of populations. In genome-wide association studies C4 deficiencies are missed because the genetic variation of C4 is complex. There are no studies where the clinical presentation of these patients is analyzed. This...
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| Publicado no: | PLoS One |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6013154/ https://ncbi.nlm.nih.gov/pubmed/29928053 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0199305 |
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