Description:
COCKAYNE SYNDROME TYPE A - 216400
NIA AGING CELL REPOSITORY DNA PANEL - AGING SYNDROMES
|
Repository
|
No Data
|
| Subcollection |
Heritable Diseases |
|
License Required
|
No Data
|
| Class |
Repair Defective and Chromosomal Instability Syndromes |
|
Sample Source
|
No Data
|
|
Subject Type
|
No Data
|
|
Family Type
|
No Data
|
|
Ethnicity
|
No Data
|
|
Family Member
|
No Data
|
|
Genetic Data
|
No Data
|
| Passage Frozen |
10 |
| |
| IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Chromosome Analysis |
| |
| Tuo J, Jaruga P, Rodriguez H, Bohr VA, Dizdaroglu M, Primary fibroblasts of Cockayne syndrome patients are defective in cellular
repair of 8-hydroxyguanine and 8-hydroxyadenine resulting from oxidative stress. FASEB J17(6):668-74 2003 |
| PubMed ID: 12665480 |
| |
| Levinson ED, Zimmerman AW, Grunnet ML, Lewis RA, Spackman TJ, Cockayne syndrome. J Comput Assist Tomogr6:1172-4 1982 |
| PubMed ID: 7174933 |
|
|