about
Myosin heavy chain-9-related disorders (MYH9-RD): a case report.Ventricular septal defect in a child with Alport syndrome: a case report.Aetiological investigations of hearing loss in childhood: a review.Medical genetics: 3. An approach to the adult with a genetic disorder.Improving mutation screening in familial hematuric nephropathies through next generation sequencing.Advances in Alport syndrome diagnosis using next-generation sequencingThe Accumulation of VEGFA in the Glomerular Basement Membrane and Its Relationship with Podocyte Injury and Proteinuria in Alport Syndrome.Integrin alpha1beta1 and transforming growth factor-beta1 play distinct roles in alport glomerular pathogenesis and serve as dual targets for metabolic therapy.Progression of Alport Kidney Disease in Col4a3 Knock Out Mice Is Independent of Sex or Macrophage Depletion by Clodronate TreatmentDeafness in children: a national survey of aetiological investigations.Antigen retrieval with protease digestion applied in immunohistochemical diagnosis of Alport syndrome.Global gene expression analysis reveals a role for the alpha 1 integrin in renal pathogenesis.Alport syndrome in a Kazakh family: a case study.Alport syndrome and leiomyomatosis: the first deletion extending beyond COL4A6 intron 2.
P2860
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P2860
description
1997 nî lūn-bûn
@nan
1997 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Alport's syndrome.
@ast
Alport's syndrome.
@en
type
label
Alport's syndrome.
@ast
Alport's syndrome.
@en
prefLabel
Alport's syndrome.
@ast
Alport's syndrome.
@en
P2860
P356
P1476
Alport's syndrome.
@en
P2093
P2860
P304
P356
10.1136/JMG.34.4.326
P407
P577
1997-04-01T00:00:00Z