A prevalent C3 mutation in aHUS patients causes a direct C3 convertase gain of function

LT Roumenina, M Frimat, EC Miller… - Blood, The Journal …, 2012 - ashpublications.org
Atypical hemolytic uremic syndrome (aHUS) is a rare renal thrombotic microangiopathy
commonly associated with rare genetic variants in complement system genes, unique to …

Aprevalent C3 mutation in aHUS patients causes a direct C3 convertase gain offunction

LT Roumenina, M Frimat, EC Miller, F Provot… - Blood, 2012 - profiles.wustl.edu
Atypical hemolytic uremic syndrome (aHUS) is a rare renal thrombotic microangiopathy
commonly associated with rare genetic variants in complement system genes, unique to …

A prevalent C3 mutation in aHUS patients causes a direct C3 convertase gain of function

LT Roumenina, M Frimat, EC Miller, F Provot… - Blood, 2012 - cir.nii.ac.jp
抄録< jats: title> Abstract</jats: title>< jats: p> Atypical hemolytic uremic syndrome (aHUS) is
a rare renal thrombotic microangiopathy commonly associated with rare genetic variants in …

[PDF][PDF] A prevalent C3 mutation in aHUS patients causes a direct C3 convertase gain of function

LT Roumenina, M Frimat, EC Miller, F Provot… - BLOOD, 2012 - academia.edu
Atypical hemolytic uremic syndrome (aHUS) is a rare renal thrombotic microangiopathy
commonly associated with rare genetic variants in complement system genes, unique to …

A prevalent C3 mutation in aHUS patients causes a direct C3 convertase gain of function.

LT Roumenina, M Frimat, EC Miller, F Provot… - Blood, 2012 - europepmc.org
Atypical hemolytic uremic syndrome (aHUS) is a rare renal thrombotic microangiopathy
commonly associated with rare genetic variants in complement system genes, unique to …

A prevalent C3 mutation in aHUS patients causes a direct C3 convertase gain of function

LT Roumenina, M Frimat, EC Miller, F Provot… - …, 2012 - research-information.bris.ac.uk
Atypical hemolytic uremic syndrome (aHUS) is a rare renal thrombotic microangiopathy
commonly associated with rare genetic variants in complement system genes, unique to …

[HTML][HTML] A prevalent C3 mutation in aHUS patients causes a direct C3 convertase gain of function

LT Roumenina, M Frimat, EC Miller, F Provot… - Blood, 2012 - Elsevier
Atypical hemolytic uremic syndrome (aHUS) is a rare renal thrombotic microangiopathy
commonly associated with rare genetic variants in complement system genes, unique to …

[引用][C] A prevalent C3 mutation in aHUS patients causes a direct C3 convertase gain of function

LT ROUMENINA, M FRIMAT, C MOUSSON, C NOEL… - Blood, 2012 - pascal-francis.inist.fr
A prevalent C3 mutation in aHUS patients causes a direct C3 convertase gain of function
CNRS Inist Pascal-Francis CNRS Pascal and Francis Bibliographic Databases Simple …

Aprevalent C3 mutation in aHUS patients causes a direct C3 convertase gain offunction

LT Roumenina, M Frimat, EC Miller, F Provot… - Blood, 2012 - hub.hku.hk
Atypical hemolytic uremic syndrome (aHUS) is a rare renal thrombotic microangiopathy
commonly associated with rare genetic variants in complement system genes, unique to …

[PDF][PDF] A prevalent C3 mutation in aHUS patients causes a direct C3 convertase gain of function

LT Roumenina, M Frimat, EC Miller, F Provot… - BLOOD, 2012 - researchgate.net
Atypical hemolytic uremic syndrome (aHUS) is a rare renal thrombotic microangiopathy
commonly associated with rare genetic variants in complement system genes, unique to …