Restricted genetic defects underlie human complement C6 deficiency

Complement C6 homozygous deficiency (C6D) has been rarely observed in Caucasians but was reported at higher prevalence among African-Americans. We report on the molecular basis of C6D in seven unrelated black individuals of North or Central Africa descent who live in France. These patients have pres...

Popoln opis

Shranjeno v:
Bibliografske podrobnosti
Main Authors: DRAGON-DUREY, M A, FREMEAUX-BACCHI, V, BLOUIN, J, BARRAUD, D, FRIDMAN, W H, KAZATCHKINE, M D
Format: Artigo
Jezik:Inglês
Izdano: Blackwell Science Inc 2003
Teme:
Original Articles
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC1808670/
https://ncbi.nlm.nih.gov/pubmed/12653841
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1046/j.1365-2249.2003.02099.x
Oznake: Označite
Brez oznak, prvi označite!

Podobne knjige/članki