A novel splice site mutation in the Cockayne syndrome group A gene in two siblings with Cockayne syndrome.
about
A UV-sensitive syndrome patient with a specific CSA mutation reveals separable roles for CSA in response to UV and oxidative DNA damageIncidence rates of progressive childhood encephalopathy in Oslo, Norway: a population based study.Cockayne syndrome group B protein is engaged in processing of DNA adducts of lipid peroxidation product trans-4-hydroxy-2-nonenalMolecular spectrum of excision repair cross-complementation group 8 gene defects in Chinese patients with Cockayne syndrome type A.
P2860
A novel splice site mutation in the Cockayne syndrome group A gene in two siblings with Cockayne syndrome.
description
2006 nî lūn-bûn
@nan
2006 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
A novel splice site mutation i ...... blings with Cockayne syndrome.
@ast
A novel splice site mutation i ...... blings with Cockayne syndrome.
@en
type
label
A novel splice site mutation i ...... blings with Cockayne syndrome.
@ast
A novel splice site mutation i ...... blings with Cockayne syndrome.
@en
prefLabel
A novel splice site mutation i ...... blings with Cockayne syndrome.
@ast
A novel splice site mutation i ...... blings with Cockayne syndrome.
@en
P2093
P1433
P1476
A novel splice site mutation i ...... blings with Cockayne syndrome.
@en
P2093
P304
P356
10.1016/J.NEUROSCIENCE.2006.09.025
P407
P577
2006-11-02T00:00:00Z