Recurrent mutation in the crystallin alpha A gene associated with inherited paediatric cataract.
about
Correlations of single nucleotide polymorphisms of CRYAA and CRYAB genes with the risk and clinicopathological features of children suffering from congenital cataract.Inherited Congenital Cataract: A Guide to Suspect the Genetic Etiology in the Cataract Genesis.High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia.Two novel mutations identified in ADCC families impair crystallin protein distribution and induce apoptosis in human lens epithelial cells.Genes and genetics in eye diseases: a genomic medicine approach for investigating hereditary and inflammatory ocular disorders.αA-crystallin-derived minichaperone stabilizes αAG98R-crystallin by affecting its zeta potential.
P2860
Recurrent mutation in the crystallin alpha A gene associated with inherited paediatric cataract.
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
Recurrent mutation in the crys ...... inherited paediatric cataract.
@ast
Recurrent mutation in the crys ...... inherited paediatric cataract.
@en
type
label
Recurrent mutation in the crys ...... inherited paediatric cataract.
@ast
Recurrent mutation in the crys ...... inherited paediatric cataract.
@en
prefLabel
Recurrent mutation in the crys ...... inherited paediatric cataract.
@ast
Recurrent mutation in the crys ...... inherited paediatric cataract.
@en
P2093
P2860
P50
P1433
P1476
Recurrent mutation in the crys ...... inherited paediatric cataract
@en
P2093
John Pater
Shari Javadiyan
Shiwani Sharma
Theresa Casey
Trevor Hodson
P2860
P2888
P356
10.1186/S13104-016-1890-0
P577
2016-02-11T00:00:00Z
P5875
P6179
1029476961