Werner Syndrome Caused by Homozygous Frameshift Variant c.1578del in WRN

Werner Syndrome Caused by Homozygous Frameshift Variant c.1578del in WRN

Background. Progerias are rare hereditary genetic disorders that cause the onset of aging to occur earlier than generally expected, which initiates the progression of many age-related diseases. Syndromes assigned to this group are usually a compound disturbance of multiple systems. Werner syndrome...

Full description

Saved in:
Bibliographic Details
Main Authors: Jovita Patricija Druta, Gunda Petraitytė, Aušra Sasnauskienė, Eglė Preikšaitienė
Format: Article
Language:English
Published: Vilnius University Press 2024-12-01
Series:Acta Medica Lituanica
Subjects:
Progeroid syndromes
Werner syndrome
WRN gene
premature aging
Online Access:https://www.zurnalai.vu.lt/AML/article/view/35473
Tags: Add Tag
No Tags, Be the first to tag this record!

Internet

https://www.zurnalai.vu.lt/AML/article/view/35473

Similar Items