WDR73 Mutations Cause Infantile Neurodegeneration and Variable Glomerular Kidney Disease.
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Genetic testing in steroid-resistant nephrotic syndrome: when and how?Exploring the genetic basis of early-onset chronic kidney disease.Proteinuria and hematuria in the neonate.Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly.An Amish founder mutation disrupts a PI(3)P-WHAMM-Arp2/3 complex-driven autophagosomal remodeling pathway.Collapsing Glomerulopathy in a Child with Galloway-Mowat Syndrome.Extending the ophthalmological phenotype of Galloway-Mowat syndrome with distinct retinal dysfunction: a report and review of ocular findings.
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WDR73 Mutations Cause Infantile Neurodegeneration and Variable Glomerular Kidney Disease.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
WDR73 Mutations Cause Infantile Neurodegeneration and Variable Glomerular Kidney Disease.
@ast
WDR73 Mutations Cause Infantile Neurodegeneration and Variable Glomerular Kidney Disease.
@en
type
label
WDR73 Mutations Cause Infantile Neurodegeneration and Variable Glomerular Kidney Disease.
@ast
WDR73 Mutations Cause Infantile Neurodegeneration and Variable Glomerular Kidney Disease.
@en
prefLabel
WDR73 Mutations Cause Infantile Neurodegeneration and Variable Glomerular Kidney Disease.
@ast
WDR73 Mutations Cause Infantile Neurodegeneration and Variable Glomerular Kidney Disease.
@en
P2093
P2860
P50
P356
P1433
P1476
WDR73 Mutations Cause Infantile Neurodegeneration and Variable Glomerular Kidney Disease.
@en
P2093
Andreas Hahn
Andreas R Janecke
André Mégarbané
Berthold Streubel
Carolin E Sadowski
Christel Castro
Dagmar Csaicsich
Dagmar Wieczorek
Daniela Prayer
Friedhelm Hildebrandt
P2860
P304
P356
10.1002/HUMU.22828
P577
2015-06-29T00:00:00Z