NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
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Sonographic Diagnosis in a Rare Aetiology of Neonatal Scrotal Swellings: A Case Report of Congenital Nephrotic SyndromeNephrin Signaling in the Podocyte: An Updated View of Signal Regulation at the Slit Diaphragm and Beyond.Characterization of a novel disease-associated mutation within NPHS1 and its effects on nephrin phosphorylation and signaling
P2860
NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
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2015 nî lūn-bûn
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NPHS1 gene mutations confirm c ...... A novel mutation is described.
@en
type
label
NPHS1 gene mutations confirm c ...... A novel mutation is described.
@en
prefLabel
NPHS1 gene mutations confirm c ...... A novel mutation is described.
@en
P2093
P2860
P50
P356
P1433
P1476
NPHS1 gene mutations confirm c ...... A novel mutation is described.
@en
P2093
Andréa T Maciel-Guerra
Anna Cristina G B Lutaif
Luiz Cláudio Gonçalves de Castro
Marcela Lopes Souza
Maria Goretti Moreira Guimarães Penido
Maricilda P De Mello
Thaís Lira Cleto
P2860
P304
P356
10.1111/NEP.12667
P577
2015-11-11T00:00:00Z