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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Detalles Bibliográficos
Autores principales: Liesmaa, Inka, Paakkanen, Riitta, Järvinen, Asko, Valtonen, Ville, Lokki, Marja-Liisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6013154/
https://www.ncbi.nlm.nih.gov/pubmed/29928053
http://dx.doi.org/10.1371/journal.pone.0199305

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6013154/
https://www.ncbi.nlm.nih.gov/pubmed/29928053
http://dx.doi.org/10.1371/journal.pone.0199305

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