The expanding phenotypic spectra of kidney diseases: insights from genetic studies.
about
Alport syndrome cold cases: Missing mutations identified by exome sequencing and functional analysisIdentification of a novel collagen type IV alpha-4 (COL4A4) mutation in a Chinese family with autosomal dominant Alport syndrome using exome sequencing.Routine use of clinical exome-based next-generation sequencing for evaluation of patients with thrombotic microangiopathies.Rare diseases, rare presentations: recognizing atypical inherited kidney disease phenotypes in the age of genomicsGenomic medicine for kidney disease.Genetic Complexity of Autosomal Dominant Polycystic Kidney and Liver Diseases.
P2860
The expanding phenotypic spectra of kidney diseases: insights from genetic studies.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
@zh
2016年學術文章
@zh-hant
name
The expanding phenotypic spectra of kidney diseases: insights from genetic studies.
@en
type
label
The expanding phenotypic spectra of kidney diseases: insights from genetic studies.
@en
prefLabel
The expanding phenotypic spectra of kidney diseases: insights from genetic studies.
@en
P2093
P2860
P356
P1476
The expanding phenotypic spectra of kidney diseases: insights from genetic studies.
@en
P2093
Albertien M van Eerde
Franz Schaefer
Kirsten Y Renkema
Nine V A M Knoers
P2860
P2888
P304
P356
10.1038/NRNEPH.2016.87
P407
P577
2016-07-04T00:00:00Z
P6179
1034483232