載入...
Xeroderma pigmentosum complementation group G associated with Cockayne syndrome.
Xeroderma pigmentosum (XP) and Cockayne syndrome (CS) are two rare inherited disorders with a clinical and cellular hypersensitivity to the UV component of the sunlight spectrum. Although the two traits are generally considered as clinically and genetically distinct entities, on the biochemical leve...
Na minha lista:
| Main Authors: | , , , , |
|---|---|
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
1993
|
| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1682247/ https://ncbi.nlm.nih.gov/pubmed/8317483 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|