The identification of a novel splicing mutation in C1qB in a Japanese family with C1q deficiency: a case report.
about
Early Components of the Complement Classical Activation Pathway in Human Systemic Autoimmune DiseasesThe complement system in systemic lupus erythematosus: an update.Progress with the use of monoclonal antibodies for the treatment of systemic lupus erythematosus."Association of rs172378 C1q gene cluster polymorphism with lupus nephritis in Bulgarian patients".Systemic lupus erythematosus with C1q deficiency: treatment with fresh frozen plasma.
P2860
The identification of a novel splicing mutation in C1qB in a Japanese family with C1q deficiency: a case report.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 28 October 2013
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
The identification of a novel ...... C1q deficiency: a case report.
@en
The identification of a novel ...... C1q deficiency: a case report.
@nl
type
label
The identification of a novel ...... C1q deficiency: a case report.
@en
The identification of a novel ...... C1q deficiency: a case report.
@nl
prefLabel
The identification of a novel ...... C1q deficiency: a case report.
@en
The identification of a novel ...... C1q deficiency: a case report.
@nl
P2093
P2860
P356
P1476
The identification of a novel ...... C1q deficiency: a case report
@en
P2093
Etsuko Kitano
Hajime Kitamura
Hidetoshi Takada
Junya Shimizu
Kenji Asagoe
Masataka Ishimura
Michiyo Hatanaka
Toshihide Kubo
Toshiro Hara
Yousuke Higuchi
P2860
P2888
P356
10.1186/1546-0096-11-41
P50
P577
2013-10-28T00:00:00Z
P5875
P6179
1048826253