Collagen type IV-related nephropathies in Portugal: pathogenic COL4A3 and COL4A4 mutations and clinical characterization of 25 families.
about
ANCA vasculitis in a patient with Alport syndrome: a difficult diagnosis but a treatable disease!Mutation analysis of COL4A3 and COL4A4 genes in a Chinese autosomal-dominant Alport syndrome family.Frequent COL4 mutations in familial microhematuria accompanied by later-onset Alport nephropathy due to focal segmental glomerulosclerosis.Collagen type IV-related nephropathies in Portugal: pathogenic COL4A5 mutations and clinical characterization of 22 families.
P2860
Collagen type IV-related nephropathies in Portugal: pathogenic COL4A3 and COL4A4 mutations and clinical characterization of 25 families.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年学术文章
@wuu
2014年学术文章
@zh
2014年学术文章
@zh-cn
2014年学术文章
@zh-hans
2014年学术文章
@zh-my
2014年学术文章
@zh-sg
2014年學術文章
@yue
2014年學術文章
@zh-hant
name
Collagen type IV-related nephr ...... aracterization of 25 families.
@en
Collagen type IV-related nephr ...... aracterization of 25 families.
@nl
type
label
Collagen type IV-related nephr ...... aracterization of 25 families.
@en
Collagen type IV-related nephr ...... aracterization of 25 families.
@nl
prefLabel
Collagen type IV-related nephr ...... aracterization of 25 families.
@en
Collagen type IV-related nephr ...... aracterization of 25 families.
@nl
P2093
P2860
P50
P356
P1433
P1476
Collagen type IV-related nephr ...... aracterization of 25 families.
@en
P2093
A C Henriques
A G da Costa
A Oliveira
C P de Moura
F Carvalho
J A Araújo
J P Oliveira
P2860
P304
P356
10.1111/CGE.12521
P577
2014-10-13T00:00:00Z