Yüklüyor......

Cockayne Syndrome Group B Cellular and Biochemical Functions

The devastating genetic disorder Cockayne syndrome (CS) arises from mutations in the CSA and CSB genes. CS is characterized by progressive multisystem degeneration and is classified as a segmental premature-aging syndrome. The CS complementation group B (CSB) protein is at the interface of transcrip...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Licht, Cecilie Löe, Stevnsner, Tinna, Bohr, Vilhelm A.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: The American Society of Human Genetics 2003
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1180389/
https://ncbi.nlm.nih.gov/pubmed/14639525
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!