MAGI2 Mutations Cause Congenital Nephrotic Syndrome.

MAGI2 Mutations Cause Congenital Nephrotic Syndrome.

Item
http://www.wikidata.org/entity/Q39118036
Clinical genetic testing using a custom-designed steroid-resistant nephrotic syndrome gene panel: analysis and recommendations.Using the Drosophila Nephrocyte to Model Podocyte Function and Disease.Genetic testing in steroid-resistant nephrotic syndrome: why, who, when and how?Glomerulosclerosis Induced by Deficiency of Membrane-Associated Guanylate Kinase Inverted 2 in Kidney Podocytes.A Multi-layered Quantitative In Vivo Expression Atlas of the Podocyte Unravels Kidney Disease Candidate Genes.Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment.Structural Basis of Highly Specific Interaction between Nephrin and MAGI1 in Slit Diaphragm Assembly and SignalingA case report of CRB2 mutation identified in a Chinese boy with focal segmental glomerulosclerosis
P2860

MAGI2 Mutations Cause Congenital Nephrotic Syndrome.

Item
http://www.wikidata.org/entity/Q39118036
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
MAGI2 Mutations Cause Congenital Nephrotic Syndrome.
@en
MAGI2 Mutations Cause Congenital Nephrotic Syndrome.
@nl
type
label
MAGI2 Mutations Cause Congenital Nephrotic Syndrome.
@en
MAGI2 Mutations Cause Congenital Nephrotic Syndrome.
@nl
prefLabel
MAGI2 Mutations Cause Congenital Nephrotic Syndrome.
@en
MAGI2 Mutations Cause Congenital Nephrotic Syndrome.
@nl
P1433
P1476
P2093
P2860
P304
P31
P356
P433
P478
P50
P577
P698
P921
P932
P356
P1433
P1476
MAGI2 Mutations Cause Congenital Nephrotic Syndrome.
@en
P2093
P2860
P304
P31
P356
P433
P478
P50
P577
P698
P921
P932