Prenatal diagnosis of heterozygous deficiency of the second component of complement.
Genetically determined C2 deficiency predisposes an individual to recurrent and invasive bacterial infections as well as a variety of rheumatic diseases. Most C2-deficient individuals carry the same 28-bp deletion in the sixth exon of the C2 gene. The present article reports the first prenatal analy...
Guardat en:
| Publicat a: | Clin Diagn Lab Immunol |
|---|---|
| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society for Microbiology (ASM)
1994
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC368348/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8556508/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/cdli.1.5.606-607.1994 |
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